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rs118109635

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs118109635(A;A)
Make rs118109635(A;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position168944621
GeneABCB11
is asnp
is mentioned by
dbSNPrs118109635
ebirs118109635
HLIrs118109635
Exacrs118109635
Varsomers118109635
Maprs118109635
PheGenIrs118109635
hapmaprs118109635
1000 genomesrs118109635
hgdprs118109635
ensemblrs118109635
gopubmedrs118109635
geneviewrs118109635
scholarrs118109635
googlers118109635
pharmgkbrs118109635
gwascentralrs118109635
openSNPrs118109635
23andMers118109635
23andMe allrs118109635
SNP Nexus

SNPshotrs118109635
SNPdbers118109635
MSV3drs118109635
GWAS Ctlgrs118109635
Max Magnitude0

[PMID 25323205] Variations of ABCB4 and ABCB11 genes are associated with primary intrahepatic stones

ClinVar
Risk rs118109635(A;A)
Alt rs118109635(A;A)
Reference rs118109635(G;G)
Significance Probable-non-pathogenic
Disease not provided
Variation info
Gene ABCB11
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.169801131G>A
CLNSRC
CLNACC RCV000224014.1,