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rs63751646

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751646(A;T)
Make rs63751646(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47445559
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751646
ebirs63751646
HLIrs63751646
Exacrs63751646
Varsomers63751646
Maprs63751646
PheGenIrs63751646
hapmaprs63751646
1000 genomesrs63751646
hgdprs63751646
ensemblrs63751646
gopubmedrs63751646
geneviewrs63751646
scholarrs63751646
googlers63751646
pharmgkbrs63751646
gwascentralrs63751646
openSNPrs63751646
23andMers63751646
23andMe allrs63751646
SNP Nexus

SNPshotrs63751646
SNPdbers63751646
MSV3drs63751646
GWAS Ctlgrs63751646
Max Magnitude0
ClinVar
Risk rs63751646(T;T)
Alt rs63751646(T;T)
Reference rs63751646(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47672698A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076114.2,