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rs63749913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs63749913(-;-)
Make rs63749913(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478351
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749913
ebirs63749913
HLIrs63749913
Exacrs63749913
Varsomers63749913
Maprs63749913
PheGenIrs63749913
hapmaprs63749913
1000 genomesrs63749913
hgdprs63749913
ensemblrs63749913
gopubmedrs63749913
geneviewrs63749913
scholarrs63749913
googlers63749913
pharmgkbrs63749913
gwascentralrs63749913
openSNPrs63749913
23andMers63749913
23andMe allrs63749913
SNP Nexus

SNPshotrs63749913
SNPdbers63749913
MSV3drs63749913
GWAS Ctlgrs63749913
Max Magnitude0
ClinVar
Risk rs63749913(;)
Alt rs63749913(;)
Reference rs63749913(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705490delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076449.2,