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

rs63750909

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750909(C;T)
Make rs63750909(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799427
GeneMSH6
is asnp
is mentioned by
dbSNPrs63750909
ebirs63750909
HLIrs63750909
Exacrs63750909
Varsomers63750909
Maprs63750909
PheGenIrs63750909
hapmaprs63750909
1000 genomesrs63750909
hgdprs63750909
ensemblrs63750909
gopubmedrs63750909
geneviewrs63750909
scholarrs63750909
googlers63750909
pharmgkbrs63750909
gwascentralrs63750909
openSNPrs63750909
23andMers63750909
23andMe allrs63750909
SNP Nexus

SNPshotrs63750909
SNPdbers63750909
MSV3drs63750909
GWAS Ctlgrs63750909
Max Magnitude0
ClinVar
Risk rs63750909(A,T;A,T)
Alt rs63750909(A,T;A,T)
Reference rs63750909(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48026566C>A; NC_000002.11:g.48026566C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000163642.1, RCV000074656.2, RCV000215386.1,