Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751133

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
(TG;TG) 0 common in clinvar
Make rs63751133(-;-)
Make rs63751133(-;GT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47414286
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751133
ebirs63751133
HLIrs63751133
Exacrs63751133
Varsomers63751133
Maprs63751133
PheGenIrs63751133
hapmaprs63751133
1000 genomesrs63751133
hgdprs63751133
ensemblrs63751133
gopubmedrs63751133
geneviewrs63751133
scholarrs63751133
googlers63751133
pharmgkbrs63751133
gwascentralrs63751133
openSNPrs63751133
23andMers63751133
23andMe allrs63751133
SNP Nexus

SNPshotrs63751133
SNPdbers63751133
MSV3drs63751133
GWAS Ctlgrs63751133
Max Magnitude0
ClinVar
Risk rs63751133(;)
Alt rs63751133(;)
Reference rs63751133(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641425_47641426delGT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076725.2,