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rs63750583

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs63750583(CT;CT)
Make rs63750583(CT;GC)
ReferenceGRCh38 38.1/141
Chromosome2
Position47463120
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750583
ebirs63750583
HLIrs63750583
Exacrs63750583
Varsomers63750583
Maprs63750583
PheGenIrs63750583
hapmaprs63750583
1000 genomesrs63750583
hgdprs63750583
ensemblrs63750583
gopubmedrs63750583
geneviewrs63750583
scholarrs63750583
googlers63750583
pharmgkbrs63750583
gwascentralrs63750583
openSNPrs63750583
23andMers63750583
23andMe allrs63750583
SNP Nexus

SNPshotrs63750583
SNPdbers63750583
MSV3drs63750583
GWAS Ctlgrs63750583
Max Magnitude0
ClinVar
Risk rs63750583(CT;CT)
Alt rs63750583(CT;CT)
Reference rs63750583(GC;GC)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690259_47690260delGCinsCT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076172.2,