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rs764958537

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs764958537(C;C)
Make rs764958537(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position99817338
GeneABCC2
is asnp
is mentioned by
dbSNPrs764958537
dbSNP (old)rs764958537
ClinGenrs764958537
ebirs764958537
HLIrs764958537
Exacrs764958537
Gnomadrs764958537
Varsomers764958537
Maprs764958537
PheGenIrs764958537
Biobankrs764958537
1000 genomesrs764958537
hgdprs764958537
ensemblrs764958537
gopubmedrs764958537
geneviewrs764958537
scholarrs764958537
googlers764958537
pharmgkbrs764958537
gwascentralrs764958537
openSNPrs764958537
23andMers764958537
23andMe allrs764958537
SNPshotrs764958537
SNPdbers764958537
MSV3drs764958537
GWAS Ctlgrs764958537
Max Magnitude0
ClinVar
Risk rs764958537(C;C)
Alt rs764958537(C;C)
Reference Rs764958537(T;T)
Significance Pathogenic
Disease Dubin-Johnson syndrome
Variation info
Gene ABCC2
CLNDBN Dubin-Johnson syndrome
Reversed 0
HGVS NC_000010.10:g.101577095T>C
CLNSRC
CLNACC RCV000391369.1,