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rs63750682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(I;I) 0
Make rs63750682(-;-)
Make rs63750682(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410314
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750682
ebirs63750682
HLIrs63750682
Exacrs63750682
Varsomers63750682
Maprs63750682
PheGenIrs63750682
hapmaprs63750682
1000 genomesrs63750682
hgdprs63750682
ensemblrs63750682
gopubmedrs63750682
geneviewrs63750682
scholarrs63750682
googlers63750682
pharmgkbrs63750682
gwascentralrs63750682
openSNPrs63750682
23andMers63750682
23andMe allrs63750682
SNP Nexus

SNPshotrs63750682
SNPdbers63750682
MSV3drs63750682
GWAS Ctlgrs63750682
Max Magnitude0
ClinVar
Risk rs63750682(;)
Alt rs63750682(;)
Reference rs63750682(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637453delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076646.2,