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rs754287486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754287486(A;A)
Make rs754287486(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position87452954
GeneABCB4
is asnp
is mentioned by
dbSNPrs754287486
dbSNP (classic)rs754287486
ClinGenrs754287486
ebirs754287486
HLIrs754287486
Exacrs754287486
Gnomadrs754287486
Varsomers754287486
LitVarrs754287486
Maprs754287486
PheGenIrs754287486
Biobankrs754287486
1000 genomesrs754287486
hgdprs754287486
ensemblrs754287486
geneviewrs754287486
scholarrs754287486
googlers754287486
pharmgkbrs754287486
gwascentralrs754287486
openSNPrs754287486
23andMers754287486
23andMe allrs754287486
SNPshotrs754287486
SNPdbers754287486
MSV3drs754287486
GWAS Ctlgrs754287486
Max Magnitude0
ClinVar
Risk rs754287486(A;A)
Alt rs754287486(A;A)
Reference Rs754287486(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCB4
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.87082270G>A
CLNSRC
CLNACC RCV000414549.1,