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rs63750107

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63750107(-;-)
Make rs63750107(-;G)
Make rs63750107(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47412503
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750107
ebirs63750107
HLIrs63750107
Exacrs63750107
Varsomers63750107
Maprs63750107
PheGenIrs63750107
hapmaprs63750107
1000 genomesrs63750107
hgdprs63750107
ensemblrs63750107
gopubmedrs63750107
geneviewrs63750107
scholarrs63750107
googlers63750107
pharmgkbrs63750107
gwascentralrs63750107
openSNPrs63750107
23andMers63750107
23andMe allrs63750107
SNP Nexus

SNPshotrs63750107
SNPdbers63750107
MSV3drs63750107
GWAS Ctlgrs63750107
Max Magnitude0
ClinVar
Risk rs63750107(G;G)
Alt rs63750107(G;G)
Reference rs63750107(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639642dupG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076694.2,