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rs72558202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558202(A;G)
Make rs72558202(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position99845781
GeneABCC2
is asnp
is mentioned by
dbSNPrs72558202
ebirs72558202
HLIrs72558202
Exacrs72558202
Varsomers72558202
Maprs72558202
PheGenIrs72558202
hapmaprs72558202
1000 genomesrs72558202
hgdprs72558202
ensemblrs72558202
gopubmedrs72558202
geneviewrs72558202
scholarrs72558202
googlers72558202
pharmgkbrs72558202
gwascentralrs72558202
openSNPrs72558202
23andMers72558202
23andMe allrs72558202
SNP Nexus

SNPshotrs72558202
SNPdbers72558202
MSV3drs72558202
GWAS Ctlgrs72558202
Max Magnitude0
OMIM601107
Desc
Variant0005
Relatedalso


ClinVar
Risk rs72558202(G;G)
Alt rs72558202(G;G)
Reference rs72558202(A;A)
Significance Pathogenic
Disease Dubin-Johnson syndrome
Variation info
Gene ABCC2
CLNDBN Dubin-Johnson syndrome
Reversed 0
HGVS NC_000010.10:g.101605538A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008927.4,