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rs63751117

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751117(-;-)
Make rs63751117(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47480722
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751117
ebirs63751117
HLIrs63751117
Exacrs63751117
Varsomers63751117
Maprs63751117
PheGenIrs63751117
hapmaprs63751117
1000 genomesrs63751117
hgdprs63751117
ensemblrs63751117
gopubmedrs63751117
geneviewrs63751117
scholarrs63751117
googlers63751117
pharmgkbrs63751117
gwascentralrs63751117
openSNPrs63751117
23andMers63751117
23andMe allrs63751117
SNP Nexus

SNPshotrs63751117
SNPdbers63751117
MSV3drs63751117
GWAS Ctlgrs63751117
Max Magnitude0
ClinVar
Risk rs63751117(;)
Alt rs63751117(;)
Reference rs63751117(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47707861delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076487.2,