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rs63750872

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750872(A;A)
Make rs63750872(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476452
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750872
ebirs63750872
HLIrs63750872
Exacrs63750872
Varsomers63750872
Maprs63750872
PheGenIrs63750872
hapmaprs63750872
1000 genomesrs63750872
hgdprs63750872
ensemblrs63750872
gopubmedrs63750872
geneviewrs63750872
scholarrs63750872
googlers63750872
pharmgkbrs63750872
gwascentralrs63750872
openSNPrs63750872
23andMers63750872
23andMe allrs63750872
SNP Nexus

SNPshotrs63750872
SNPdbers63750872
MSV3drs63750872
GWAS Ctlgrs63750872
Max Magnitude0
ClinVar
Risk rs63750872(A;A)
Alt rs63750872(A;A)
Reference rs63750872(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703591T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076386.2,