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rs72558201

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558201(A;T)
Make rs72558201(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position99836193
GeneABCC2
is asnp
is mentioned by
dbSNPrs72558201
ebirs72558201
HLIrs72558201
Exacrs72558201
Varsomers72558201
Maprs72558201
PheGenIrs72558201
hapmaprs72558201
1000 genomesrs72558201
hgdprs72558201
ensemblrs72558201
gopubmedrs72558201
geneviewrs72558201
scholarrs72558201
googlers72558201
pharmgkbrs72558201
gwascentralrs72558201
openSNPrs72558201
23andMers72558201
23andMe allrs72558201
SNP Nexus

SNPshotrs72558201
SNPdbers72558201
MSV3drs72558201
GWAS Ctlgrs72558201
Max Magnitude0
OMIM601107
Desc
Variant0007
Relatedalso
ClinVar
Risk rs72558201(G,T;G,T)
Alt rs72558201(G,T;G,T)
Reference rs72558201(A;A)
Significance Pathogenic
Disease Dubin-Johnson syndrome
Variation info
Gene ABCC2
CLNDBN Dubin-Johnson syndrome
Reversed 0
HGVS NC_000010.10:g.101595950A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008929.3,