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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

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