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rs387906395

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906395(A;A)
Make rs387906395(A;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position99808231
GeneABCC2
is asnp
is mentioned by
dbSNPrs387906395
ebirs387906395
HLIrs387906395
Exacrs387906395
Varsomers387906395
Maprs387906395
PheGenIrs387906395
hapmaprs387906395
1000 genomesrs387906395
hgdprs387906395
ensemblrs387906395
gopubmedrs387906395
geneviewrs387906395
scholarrs387906395
googlers387906395
pharmgkbrs387906395
gwascentralrs387906395
openSNPrs387906395
23andMers387906395
23andMe allrs387906395
SNP Nexus

SNPshotrs387906395
SNPdbers387906395
MSV3drs387906395
GWAS Ctlgrs387906395
Max Magnitude0
ClinVar
Risk rs387906395(A;A)
Alt rs387906395(A;A)
Reference rs387906395(T;T)
Significance Pathogenic
Disease Dubin-Johnson syndrome
Variation info
Gene ABCC2
CLNDBN Dubin-Johnson syndrome
Reversed 0
HGVS NC_000010.10:g.101567988T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008925.3,