Have questions? Visit https://www.reddit.com/r/SNPedia

rs121434628

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434628(C;T)
Make rs121434628(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position189844078
GenePMS1
is asnp
is mentioned by
dbSNPrs121434628
ebirs121434628
HLIrs121434628
Exacrs121434628
Varsomers121434628
Maprs121434628
PheGenIrs121434628
hapmaprs121434628
1000 genomesrs121434628
hgdprs121434628
ensemblrs121434628
gopubmedrs121434628
geneviewrs121434628
scholarrs121434628
googlers121434628
pharmgkbrs121434628
gwascentralrs121434628
openSNPrs121434628
23andMers121434628
23andMe allrs121434628
SNP Nexus

SNPshotrs121434628
SNPdbers121434628
MSV3drs121434628
GWAS Ctlgrs121434628
Max Magnitude0
OMIM600258
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434628(T;T)
Alt rs121434628(T;T)
Reference rs121434628(C;C)
Significance Untested
Disease Hereditary nonpolyposis colorectal cancer type 3
Variation info
Gene PMS1
CLNDBN Hereditary nonpolyposis colorectal cancer type 3
Reversed 0
HGVS NC_000002.11:g.190708804C>T
CLNSRC OMIM Allelic Variant
CLNACC SCV000030052.1,