347544 RESULTS
MUTATIONS SORL1 121585947 GRCh38/hg38 rs73595281 C G 121456656 GRCh37/hg19 rs73595281 C G Intron 26 Non-Coding c.3707-275C>G Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of
MUTATIONS SORL1 121585352 GRCh38/hg38 rs117807585 G A 121456061 GRCh37/hg19 rs117807585 G A Intron 26 Non-Coding c.3707-870G>A Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk o
MUTATIONS SORL1 121583074 GRCh38/hg38 rs76490923 C T 121453783 GRCh37/hg19 rs76490923 C T Intron 25 Non-Coding c.3581-384C>T Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of
MUTATIONS SORL1 121583070 GRCh38/hg38 rs58698151 A T 121453779 GRCh37/hg19 rs58698151 A T Intron 25 Non-Coding c.3581-388A>T Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of
MUTATIONS SORL1 121581645 GRCh38/hg38 rs7120354 G A 121452354 GRCh37/hg19 rs7120354 G A Intron 25 Non-Coding c.3581-1813G>A Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of A
MUTATIONS SORL1 121580992 GRCh38/hg38 rs79829457 A G 121451701 GRCh37/hg19 rs79829457 A G Intron 25 Non-Coding c.3581-2466A>G Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of
MUTATIONS SORL1 121578263 GRCh38/hg38 rs3781837 T C 121448972 GRCh37/hg19 rs3781837 T C Intron 25 Non-Coding c.3580+863T>C Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of Al
MUTATIONS SORL1 121575890 GRCh38/hg38 rs1620130 T C 121446599 GRCh37/hg19 rs1620130 T C Intron 24 Non-Coding c.3461-1391T>C Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of A
MUTATIONS SORL1 121575509 GRCh38/hg38 rs75279208 C G 121446218 GRCh37/hg19 rs75279208 C G Intron 24 Non-Coding c.3460+1146C>G Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of
MUTATIONS SORL1 121574102 GRCh38/hg38 rs17125473 G C 121444811 GRCh37/hg19 rs17125473 G C Intron 23 Non-Coding c.3338-139G>C Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of
MUTATIONS SORL1 121566862 GRCh38/hg38 rs1784920 A G 121437571 GRCh37/hg19 rs1784920 A G Intron 21 Non-Coding c.3050-78A>G Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of Alz
MUTATIONS SORL1 121565295 GRCh38/hg38 rs3781831 G A 121436004 GRCh37/hg19 rs3781831 G A Intron 21 Non-Coding c.3050-1645G>A Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of A
MUTATIONS SORL1 121563217 GRCh38/hg38 rs80256323 C A 121433926 GRCh37/hg19 rs80256323 C A Intron 21 Non-Coding c.3049+3560C>A Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of
MUTATIONS SORL1 121562211 GRCh38/hg38 rs76604503 C T 121432920 GRCh37/hg19 rs76604503 C T Intron 21 Non-Coding c.3049+2554C>T Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of
Canada
