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rs146405172

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs146405172(A;A)
Make rs146405172(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position99811603
GeneABCC2
is asnp
is mentioned by
dbSNPrs146405172
ebirs146405172
HLIrs146405172
Exacrs146405172
Varsomers146405172
Maprs146405172
PheGenIrs146405172
hapmaprs146405172
1000 genomesrs146405172
hgdprs146405172
ensemblrs146405172
gopubmedrs146405172
geneviewrs146405172
scholarrs146405172
googlers146405172
pharmgkbrs146405172
gwascentralrs146405172
openSNPrs146405172
23andMers146405172
23andMe allrs146405172
SNP Nexus

SNPshotrs146405172
SNPdbers146405172
MSV3drs146405172
GWAS Ctlgrs146405172
Max Magnitude0
ClinVar
Risk rs146405172(A;A)
Alt rs146405172(A;A)
Reference rs146405172(G;G)
Significance Pathogenic
Disease Dubin-Johnson syndrome
Variation info
Gene ABCC2
CLNDBN Dubin-Johnson syndrome
Reversed 0
HGVS NC_000010.10:g.101571360G>A
CLNSRC
CLNACC RCV000174845.1,