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rs63751617

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751617(A;T)
Make rs63751617(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429742
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751617
ebirs63751617
HLIrs63751617
Exacrs63751617
Varsomers63751617
Maprs63751617
PheGenIrs63751617
hapmaprs63751617
1000 genomesrs63751617
hgdprs63751617
ensemblrs63751617
gopubmedrs63751617
geneviewrs63751617
scholarrs63751617
googlers63751617
pharmgkbrs63751617
gwascentralrs63751617
openSNPrs63751617
23andMers63751617
23andMe allrs63751617
SNP Nexus

SNPshotrs63751617
SNPdbers63751617
MSV3drs63751617
GWAS Ctlgrs63751617
Max Magnitude0
ClinVar
Risk rs63751617(T;T)
Alt rs63751617(T;T)
Reference rs63751617(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47656881A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076034.2,