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rs886044573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Chromosome10
Position99834520
GeneABCC2
is asnp
is mentioned by
dbSNPrs886044573
dbSNP (old)rs886044573
ClinGenrs886044573
ebirs886044573
HLIrs886044573
Exacrs886044573
Gnomadrs886044573
Varsomers886044573
Maprs886044573
PheGenIrs886044573
Biobankrs886044573
1000 genomesrs886044573
hgdprs886044573
ensemblrs886044573
gopubmedrs886044573
geneviewrs886044573
scholarrs886044573
googlers886044573
pharmgkbrs886044573
gwascentralrs886044573
openSNPrs886044573
23andMers886044573
23andMe allrs886044573
SNP Nexus

SNPshotrs886044573
SNPdbers886044573
MSV3drs886044573
GWAS Ctlgrs886044573
Max Magnitude0
ClinVar
Risk rs886044573(-;-)
Alt rs886044573(-;-)
Reference Rs886044573(TT;TT)
Significance Pathogenic
Disease Dubin-Johnson syndrome
Variation info
Gene ABCC2
CLNDBN Dubin-Johnson syndrome
Reversed 0
HGVS NC_000010.10:g.101594277_101594278delTT
CLNSRC
CLNACC RCV000366725.1,