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rs63751123

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751123(-;-)
Make rs63751123(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476371
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751123
ebirs63751123
HLIrs63751123
Exacrs63751123
Varsomers63751123
Maprs63751123
PheGenIrs63751123
hapmaprs63751123
1000 genomesrs63751123
hgdprs63751123
ensemblrs63751123
gopubmedrs63751123
geneviewrs63751123
scholarrs63751123
googlers63751123
pharmgkbrs63751123
gwascentralrs63751123
openSNPrs63751123
23andMers63751123
23andMe allrs63751123
SNP Nexus

SNPshotrs63751123
SNPdbers63751123
MSV3drs63751123
GWAS Ctlgrs63751123
Max Magnitude0
ClinVar
Risk rs63751123(;)
Alt rs63751123(;)
Reference rs63751123(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703510delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076358.2,