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rs121918714

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918714(C;C)
Make rs121918714(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position30691471
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs121918714
ebirs121918714
HLIrs121918714
Exacrs121918714
Varsomers121918714
Maprs121918714
PheGenIrs121918714
hapmaprs121918714
1000 genomesrs121918714
hgdprs121918714
ensemblrs121918714
gopubmedrs121918714
geneviewrs121918714
scholarrs121918714
googlers121918714
pharmgkbrs121918714
gwascentralrs121918714
openSNPrs121918714
23andMers121918714
23andMe allrs121918714
SNP Nexus

SNPshotrs121918714
SNPdbers121918714
MSV3drs121918714
GWAS Ctlgrs121918714
Max Magnitude0
OMIM190182
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121918714(C;C)
Alt rs121918714(C;C)
Reference rs121918714(G;G)
Significance Pathogenic
Disease Malignant tumor of esophagus
Variation info
Gene TGFBR2
CLNDBN Malignant tumor of esophagus
Reversed 0
HGVS NC_000003.11:g.30732963G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013326.5,