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rs63751667

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63751667(-;-)
Make rs63751667(-;A)
Make rs63751667(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429934
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751667
ebirs63751667
HLIrs63751667
Exacrs63751667
Varsomers63751667
Maprs63751667
PheGenIrs63751667
hapmaprs63751667
1000 genomesrs63751667
hgdprs63751667
ensemblrs63751667
gopubmedrs63751667
geneviewrs63751667
scholarrs63751667
googlers63751667
pharmgkbrs63751667
gwascentralrs63751667
openSNPrs63751667
23andMers63751667
23andMe allrs63751667
SNP Nexus

SNPshotrs63751667
SNPdbers63751667
MSV3drs63751667
GWAS Ctlgrs63751667
Max Magnitude0
ClinVar
Risk rs63751667(A;A)
Alt rs63751667(A;A)
Reference rs63751667(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657073dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076084.2,