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rs121908500

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908500(A;G)
Make rs121908500(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position13099462
GeneDLC1
is asnp
is mentioned by
dbSNPrs121908500
ebirs121908500
HLIrs121908500
Exacrs121908500
Varsomers121908500
Maprs121908500
PheGenIrs121908500
hapmaprs121908500
1000 genomesrs121908500
hgdprs121908500
ensemblrs121908500
gopubmedrs121908500
geneviewrs121908500
scholarrs121908500
googlers121908500
pharmgkbrs121908500
gwascentralrs121908500
openSNPrs121908500
23andMers121908500
23andMe allrs121908500
SNP Nexus

SNPshotrs121908500
SNPdbers121908500
MSV3drs121908500
GWAS Ctlgrs121908500
Max Magnitude0
OMIM604258
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908500(G;G)
Alt rs121908500(G;G)
Reference rs121908500(A;A)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene DLC1
CLNDBN Carcinoma of colon
Reversed 1
HGVS NC_000008.10:g.12956971T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006053.4,