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rs121913314

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913314(C;T)
Make rs121913314(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position37403359
GeneSRC
is asnp
is mentioned by
dbSNPrs121913314
ebirs121913314
HLIrs121913314
Exacrs121913314
Varsomers121913314
Maprs121913314
PheGenIrs121913314
hapmaprs121913314
1000 genomesrs121913314
hgdprs121913314
ensemblrs121913314
gopubmedrs121913314
geneviewrs121913314
scholarrs121913314
googlers121913314
pharmgkbrs121913314
gwascentralrs121913314
openSNPrs121913314
23andMers121913314
23andMe allrs121913314
SNP Nexus

SNPshotrs121913314
SNPdbers121913314
MSV3drs121913314
GWAS Ctlgrs121913314
Max Magnitude0
OMIM190090
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121913314(T;T)
Alt rs121913314(T;T)
Reference rs121913314(C;C)
Significance Pathogenic
Disease Colon cancer
Variation info
Gene SRC
CLNDBN Colon cancer, advanced
Reversed 0
HGVS NC_000020.10:g.36031762C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013401.27,