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rs63751044

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs63751044(-;-)
Make rs63751044(-;CA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47416323
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751044
ebirs63751044
HLIrs63751044
Exacrs63751044
Varsomers63751044
Maprs63751044
PheGenIrs63751044
hapmaprs63751044
1000 genomesrs63751044
hgdprs63751044
ensemblrs63751044
gopubmedrs63751044
geneviewrs63751044
scholarrs63751044
googlers63751044
pharmgkbrs63751044
gwascentralrs63751044
openSNPrs63751044
23andMers63751044
23andMe allrs63751044
SNP Nexus

SNPshotrs63751044
SNPdbers63751044
MSV3drs63751044
GWAS Ctlgrs63751044
Max Magnitude0
ClinVar
Risk rs63751044(;)
Alt rs63751044(;)
Reference rs63751044(CA;CA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47643462_47643463delCA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076767.2,