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rs63750521

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750521(G;G)
Make rs63750521(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47445644
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750521
ebirs63750521
HLIrs63750521
Exacrs63750521
Varsomers63750521
Maprs63750521
PheGenIrs63750521
hapmaprs63750521
1000 genomesrs63750521
hgdprs63750521
ensemblrs63750521
gopubmedrs63750521
geneviewrs63750521
scholarrs63750521
googlers63750521
pharmgkbrs63750521
gwascentralrs63750521
openSNPrs63750521
23andMers63750521
23andMe allrs63750521
SNP Nexus

SNPshotrs63750521
SNPdbers63750521
MSV3drs63750521
GWAS Ctlgrs63750521
Max Magnitude0
ClinVar
Risk rs63750521(G;G)
Alt rs63750521(G;G)
Reference rs63750521(T;T)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47672783T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076136.2, RCV000160582.1,