1791 RESULTS
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
