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rs146292819

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs146292819(G;G)
Make rs146292819(G;T)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position104794495
GeneABCA1
is asnp
is mentioned by
dbSNPrs146292819
dbSNP (classic)rs146292819
ClinGenrs146292819
ebirs146292819
HLIrs146292819
Exacrs146292819
Gnomadrs146292819
Varsomers146292819
LitVarrs146292819
Maprs146292819
PheGenIrs146292819
Biobankrs146292819
1000 genomesrs146292819
hgdprs146292819
ensemblrs146292819
geneviewrs146292819
scholarrs146292819
googlers146292819
pharmgkbrs146292819
gwascentralrs146292819
openSNPrs146292819
23andMers146292819
23andMe allrs146292819
SNPshotrs146292819
SNPdbers146292819
MSV3drs146292819
GWAS Ctlgrs146292819
Max Magnitude0
ClinVar
Risk rs146292819(G;G)
Alt rs146292819(G;G)
Reference Rs146292819(T;T)
Significance Pathogenic
Disease ABCA1-Related Disorders
Variation info
Gene ABCA1
CLNDBN ABCA1-Related Disorders
Reversed 0
HGVS NC_000009.11:g.107556776T>G
CLNSRC Illumina
CLNACC RCV000277325.1,