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rs752916287

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs752916287(C;G)
Make rs752916287(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position87411911
GeneABCB4
is asnp
is mentioned by
dbSNPrs752916287
ebirs752916287
HLIrs752916287
Exacrs752916287
Varsomers752916287
Maprs752916287
PheGenIrs752916287
hapmaprs752916287
1000 genomesrs752916287
hgdprs752916287
ensemblrs752916287
gopubmedrs752916287
geneviewrs752916287
scholarrs752916287
googlers752916287
pharmgkbrs752916287
gwascentralrs752916287
openSNPrs752916287
23andMers752916287
23andMe allrs752916287
SNP Nexus

SNPshotrs752916287
SNPdbers752916287
MSV3drs752916287
GWAS Ctlgrs752916287
Max Magnitude0
ClinVar
Risk rs752916287(G,T;G,T)
Alt rs752916287(G,T;G,T)
Reference rs752916287(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCB4
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.87041227C>T
CLNSRC
CLNACC RCV000171407.1,