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rs387906396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906396(C;C)
Make rs387906396(C;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position99811604
GeneABCC2
is asnp
is mentioned by
dbSNPrs387906396
ebirs387906396
HLIrs387906396
Exacrs387906396
Varsomers387906396
Maprs387906396
PheGenIrs387906396
hapmaprs387906396
1000 genomesrs387906396
hgdprs387906396
ensemblrs387906396
gopubmedrs387906396
geneviewrs387906396
scholarrs387906396
googlers387906396
pharmgkbrs387906396
gwascentralrs387906396
openSNPrs387906396
23andMers387906396
23andMe allrs387906396
SNP Nexus

SNPshotrs387906396
SNPdbers387906396
MSV3drs387906396
GWAS Ctlgrs387906396
Max Magnitude0
ClinVar
Risk rs387906396(C;C)
Alt rs387906396(C;C)
Reference rs387906396(T;T)
Significance Pathogenic
Disease Dubin-Johnson syndrome
Variation info
Gene ABCC2
CLNDBN Dubin-Johnson syndrome
Reversed 0
HGVS NC_000010.10:g.101571361T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000008928.4,