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rs72558199

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558199(C;T)
Make rs72558199(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position99832069
GeneABCC2
is asnp
is mentioned by
dbSNPrs72558199
ebirs72558199
HLIrs72558199
Exacrs72558199
Varsomers72558199
Maprs72558199
PheGenIrs72558199
hapmaprs72558199
1000 genomesrs72558199
hgdprs72558199
ensemblrs72558199
gopubmedrs72558199
geneviewrs72558199
scholarrs72558199
googlers72558199
pharmgkbrs72558199
gwascentralrs72558199
openSNPrs72558199
23andMers72558199
23andMe allrs72558199
SNP Nexus

SNPshotrs72558199
SNPdbers72558199
MSV3drs72558199
GWAS Ctlgrs72558199
Max Magnitude0
ClinVar
Risk rs72558199(T;T)
Alt rs72558199(T;T)
Reference rs72558199(C;C)
Significance Pathogenic
Disease Dubin-Johnson syndrome
Variation info
Gene ABCC2
CLNDBN Dubin-Johnson syndrome
Reversed 0
HGVS NC_000010.10:g.101591826C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000024307.3,