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rs121434587

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121434587(G;T)
Make rs121434587(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position160069961
GeneIGF2R
is asnp
is mentioned by
dbSNPrs121434587
ebirs121434587
HLIrs121434587
Exacrs121434587
Varsomers121434587
Maprs121434587
PheGenIrs121434587
hapmaprs121434587
1000 genomesrs121434587
hgdprs121434587
ensemblrs121434587
gopubmedrs121434587
geneviewrs121434587
scholarrs121434587
googlers121434587
pharmgkbrs121434587
gwascentralrs121434587
openSNPrs121434587
23andMers121434587
23andMe allrs121434587
SNP Nexus

SNPshotrs121434587
SNPdbers121434587
MSV3drs121434587
GWAS Ctlgrs121434587
Max Magnitude0
OMIM147280
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434587(T;T)
Alt rs121434587(T;T)
Reference rs121434587(G;G)
Significance Pathogenic
Disease Hepatocellular carcinoma
Variation info
Gene IGF2R
CLNDBN Hepatocellular carcinoma
Reversed 0
HGVS NC_000006.11:g.160490993G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015918.4,