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rs371866713

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs371866713(C;G)
Make rs371866713(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position99799313
GeneABCC2
is asnp
is mentioned by
dbSNPrs371866713
dbSNP (classic)rs371866713
ClinGenrs371866713
ebirs371866713
HLIrs371866713
Exacrs371866713
Gnomadrs371866713
Varsomers371866713
LitVarrs371866713
Maprs371866713
PheGenIrs371866713
Biobankrs371866713
1000 genomesrs371866713
hgdprs371866713
ensemblrs371866713
geneviewrs371866713
scholarrs371866713
googlers371866713
pharmgkbrs371866713
gwascentralrs371866713
openSNPrs371866713
23andMers371866713
23andMe allrs371866713
SNPshotrs371866713
SNPdbers371866713
MSV3drs371866713
GWAS Ctlgrs371866713
Max Magnitude0
ClinVar
Risk rs371866713(G;G)
Alt rs371866713(G;G)
Reference Rs371866713(C;C)
Significance Pathogenic
Disease Dubin-Johnson syndrome
Variation info
Gene ABCC2
CLNDBN Dubin-Johnson syndrome
Reversed 0
HGVS NC_000010.10:g.101559070C>G
CLNSRC
CLNACC RCV000343826.1,