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rs63750042

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750042(C;T)
Make rs63750042(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47408415
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750042
ebirs63750042
HLIrs63750042
Exacrs63750042
Varsomers63750042
Maprs63750042
PheGenIrs63750042
hapmaprs63750042
1000 genomesrs63750042
hgdprs63750042
ensemblrs63750042
gopubmedrs63750042
geneviewrs63750042
scholarrs63750042
googlers63750042
pharmgkbrs63750042
gwascentralrs63750042
openSNPrs63750042
23andMers63750042
23andMe allrs63750042
SNP Nexus

SNPshotrs63750042
SNPdbers63750042
MSV3drs63750042
GWAS Ctlgrs63750042
Max Magnitude0
ClinVar
Risk rs63750042(G,T;G,T)
Alt rs63750042(G,T;G,T)
Reference rs63750042(C;C)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47635554C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076447.2, RCV000202307.1,