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rs63750495

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs63750495(-;-)
Make rs63750495(-;TG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47475053
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750495
ebirs63750495
HLIrs63750495
Exacrs63750495
Varsomers63750495
Maprs63750495
PheGenIrs63750495
hapmaprs63750495
1000 genomesrs63750495
hgdprs63750495
ensemblrs63750495
gopubmedrs63750495
geneviewrs63750495
scholarrs63750495
googlers63750495
pharmgkbrs63750495
gwascentralrs63750495
openSNPrs63750495
23andMers63750495
23andMe allrs63750495
SNP Nexus

SNPshotrs63750495
SNPdbers63750495
MSV3drs63750495
GWAS Ctlgrs63750495
Max Magnitude0
ClinVar
Risk rs63750495(;)
Alt rs63750495(;)
Reference rs63750495(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47702192_47702193delTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076288.2,