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rs63751149

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63751149(A;T)
Make rs63751149(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47471002
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751149
ebirs63751149
HLIrs63751149
Exacrs63751149
Varsomers63751149
Maprs63751149
PheGenIrs63751149
hapmaprs63751149
1000 genomesrs63751149
hgdprs63751149
ensemblrs63751149
gopubmedrs63751149
geneviewrs63751149
scholarrs63751149
googlers63751149
pharmgkbrs63751149
gwascentralrs63751149
openSNPrs63751149
23andMers63751149
23andMe allrs63751149
SNP Nexus

SNPshotrs63751149
SNPdbers63751149
MSV3drs63751149
GWAS Ctlgrs63751149
Max Magnitude0
ClinVar
Risk rs63751149(G,T;G,T)
Alt rs63751149(G,T;G,T)
Reference rs63751149(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47698141A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076250.2,