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1781 RESULTS

SORL1 c.3050-2179G> A

MUTATIONS SORL1 121564761 GRCh38/hg38 rs9665907 G A 121435470 GRCh37/hg19 rs9665907 G A Intron 21 Non-Coding c.3050-2179G>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

SORL1 c.3050-2062T> C

MUTATIONS SORL1 121564878 GRCh38/hg38 rs11218343 T C 121435587 GRCh37/hg19 rs11218343 T C Intron 21 Non-Coding c.3050-2062T>C Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of

SORL1 c.3050-1379G> T

MUTATIONS SORL1 121565561 GRCh38/hg38 rs3781832 G T 121436270 GRCh37/hg19 rs3781832 G T Intron 21 Non-Coding c.3050-1379G>T Alzheimer's Disease This variant is one of 31 intronic variants in SORL1 that compose a haplotype associated with a reduced risk of A

SORL1 Haplotype A

MUTATIONS SORL1 Chromosome 11 Non-Coding Haplotype A This haplotype, composed of 31 intronic variants in SORL1, was found to be associated with a reduced risk of Alzheimer’s disease and with certain AD-related endophenotypes in people of East Asian ancestry (Zhou e

SORL1 c.3815-84G> A

MUTATIONS SORL1 121587936 GRCh38/hg38 rs17125497 G A 121458645 GRCh37/hg19 rs17125497 G A Intron 27 Non-Coding c.3815-84G>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

SORL1 c.3707-275C> G

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

SORL1 c.3707-870G> A

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

SORL1 c.3581-384C> T

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

SORL1 c.3581-388A> T

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

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