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rs63751326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751326(C;T)
Make rs63751326(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410304
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751326
ebirs63751326
HLIrs63751326
Exacrs63751326
Varsomers63751326
Maprs63751326
PheGenIrs63751326
hapmaprs63751326
1000 genomesrs63751326
hgdprs63751326
ensemblrs63751326
gopubmedrs63751326
geneviewrs63751326
scholarrs63751326
googlers63751326
pharmgkbrs63751326
gwascentralrs63751326
openSNPrs63751326
23andMers63751326
23andMe allrs63751326
SNP Nexus

SNPshotrs63751326
SNPdbers63751326
MSV3drs63751326
GWAS Ctlgrs63751326
Max Magnitude0
ClinVar
Risk rs63751326(T;T)
Alt rs63751326(T;T)
Reference rs63751326(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637443C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076645.2,