Have questions? Visit https://www.reddit.com/r/SNPedia

rs863225299

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225299(A;A)
Make rs863225299(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position87453049
GeneABCB4
is asnp
is mentioned by
dbSNPrs863225299
dbSNP (classic)rs863225299
ClinGenrs863225299
ebirs863225299
HLIrs863225299
Exacrs863225299
Gnomadrs863225299
Varsomers863225299
LitVarrs863225299
Maprs863225299
PheGenIrs863225299
Biobankrs863225299
1000 genomesrs863225299
hgdprs863225299
ensemblrs863225299
geneviewrs863225299
scholarrs863225299
googlers863225299
pharmgkbrs863225299
gwascentralrs863225299
openSNPrs863225299
23andMers863225299
SNPshotrs863225299
SNPdbers863225299
MSV3drs863225299
GWAS Ctlgrs863225299
Max Magnitude0
ClinVar
Risk rs863225299(A;A)
Alt rs863225299(A;A)
Reference Rs863225299(G;G)
Significance Probable-Pathogenic
Disease Progressive familial intrahepatic cholestasis 3
Variation info
Gene ABCB4
CLNDBN Progressive familial intrahepatic cholestasis 3
Reversed 1
HGVS NC_000007.13:g.87082365C>T
CLNSRC
CLNACC RCV000201938.1,