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rs63751226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751226(C;T)
Make rs63751226(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410199
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751226
ebirs63751226
HLIrs63751226
Exacrs63751226
Varsomers63751226
Maprs63751226
PheGenIrs63751226
hapmaprs63751226
1000 genomesrs63751226
hgdprs63751226
ensemblrs63751226
gopubmedrs63751226
geneviewrs63751226
scholarrs63751226
googlers63751226
pharmgkbrs63751226
gwascentralrs63751226
openSNPrs63751226
23andMers63751226
23andMe allrs63751226
SNP Nexus

SNPshotrs63751226
SNPdbers63751226
MSV3drs63751226
GWAS Ctlgrs63751226
Max Magnitude0
ClinVar
Risk rs63751226(T;T)
Alt rs63751226(T;T)
Reference rs63751226(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637338C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076605.2,