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rs63751274

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751274(C;T)
Make rs63751274(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410370
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751274
ebirs63751274
HLIrs63751274
Exacrs63751274
Varsomers63751274
Maprs63751274
PheGenIrs63751274
hapmaprs63751274
1000 genomesrs63751274
hgdprs63751274
ensemblrs63751274
gopubmedrs63751274
geneviewrs63751274
scholarrs63751274
googlers63751274
pharmgkbrs63751274
gwascentralrs63751274
openSNPrs63751274
23andMers63751274
23andMe allrs63751274
SNP Nexus

SNPshotrs63751274
SNPdbers63751274
MSV3drs63751274
GWAS Ctlgrs63751274
Max Magnitude0
ClinVar
Risk rs63751274(T;T)
Alt rs63751274(T;T)
Reference rs63751274(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637509C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076658.2,