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rs63751315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63751315(A;A)
Make rs63751315(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47445563
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751315
ebirs63751315
HLIrs63751315
Exacrs63751315
Varsomers63751315
Maprs63751315
PheGenIrs63751315
hapmaprs63751315
1000 genomesrs63751315
hgdprs63751315
ensemblrs63751315
gopubmedrs63751315
geneviewrs63751315
scholarrs63751315
googlers63751315
pharmgkbrs63751315
gwascentralrs63751315
openSNPrs63751315
23andMers63751315
23andMe allrs63751315
SNP Nexus

SNPshotrs63751315
SNPdbers63751315
MSV3drs63751315
GWAS Ctlgrs63751315
Max Magnitude0
ClinVar
Risk rs63751315(A;A)
Alt rs63751315(A;A)
Reference rs63751315(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47672702T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076116.2,