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rs63750712

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
(TC;TC) 0 common in clinvar
Make rs63750712(-;-)
Make rs63750712(-;CT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47408412
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750712
ebirs63750712
HLIrs63750712
Exacrs63750712
Varsomers63750712
Maprs63750712
PheGenIrs63750712
hapmaprs63750712
1000 genomesrs63750712
hgdprs63750712
ensemblrs63750712
gopubmedrs63750712
geneviewrs63750712
scholarrs63750712
googlers63750712
pharmgkbrs63750712
gwascentralrs63750712
openSNPrs63750712
23andMers63750712
23andMe allrs63750712
SNP Nexus

SNPshotrs63750712
SNPdbers63750712
MSV3drs63750712
GWAS Ctlgrs63750712
Max Magnitude0
ClinVar
Risk rs63750712(;)
Alt rs63750712(;)
Reference rs63750712(TC;TC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635551_47635552delCT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076441.2,