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rs864309675

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0 common genotype
(TG;TG) 0 common in clinvar
Make rs864309675(-;-)
Make rs864309675(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position99799352
GeneABCC2
is asnp
is mentioned by
dbSNPrs864309675
dbSNP (classic)rs864309675
ClinGenrs864309675
ebirs864309675
HLIrs864309675
Exacrs864309675
Gnomadrs864309675
Varsomers864309675
LitVarrs864309675
Maprs864309675
PheGenIrs864309675
Biobankrs864309675
1000 genomesrs864309675
hgdprs864309675
ensemblrs864309675
geneviewrs864309675
scholarrs864309675
googlers864309675
pharmgkbrs864309675
gwascentralrs864309675
openSNPrs864309675
23andMers864309675
SNPshotrs864309675
SNPdbers864309675
MSV3drs864309675
GWAS Ctlgrs864309675
Max Magnitude0
ClinVar
Risk rs864309675(-;-)
Alt rs864309675(-;-)
Reference Rs864309675(TG;TG)
Significance Pathogenic
Disease Dubin-Johnson syndrome
Variation info
Gene ABCC2
CLNDBN Dubin-Johnson syndrome
Reversed 0
HGVS NC_000010.10:g.101559109_101559110delTG
CLNSRC
CLNACC RCV000203293.1,