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rs63750704

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs63750704(-;-)
Make rs63750704(-;CA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410115
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750704
ebirs63750704
HLIrs63750704
Exacrs63750704
Varsomers63750704
Maprs63750704
PheGenIrs63750704
hapmaprs63750704
1000 genomesrs63750704
hgdprs63750704
ensemblrs63750704
gopubmedrs63750704
geneviewrs63750704
scholarrs63750704
googlers63750704
pharmgkbrs63750704
gwascentralrs63750704
openSNPrs63750704
23andMers63750704
23andMe allrs63750704
SNP Nexus

SNPshotrs63750704
SNPdbers63750704
MSV3drs63750704
GWAS Ctlgrs63750704
Max Magnitude0
ClinVar
Risk rs63750704(;)
Alt rs63750704(;)
Reference rs63750704(CA;CA)
Significance Pathogenic
Disease Lynch syndrome Colorectal cancer Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome Colorectal cancer, hereditary, nonpolyposis, type 1 Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47637254_47637255delCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC RCV000076592.2, RCV000087058.3, RCV000163755.1, RCV000235890.1,