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rs587779097

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779097(C;T)
Make rs587779097(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47466675
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779097
ebirs587779097
HLIrs587779097
Exacrs587779097
Varsomers587779097
Maprs587779097
PheGenIrs587779097
hapmaprs587779097
1000 genomesrs587779097
hgdprs587779097
ensemblrs587779097
gopubmedrs587779097
geneviewrs587779097
scholarrs587779097
googlers587779097
pharmgkbrs587779097
gwascentralrs587779097
openSNPrs587779097
23andMers587779097
23andMe allrs587779097
SNP Nexus

SNPshotrs587779097
SNPdbers587779097
MSV3drs587779097
GWAS Ctlgrs587779097
Max Magnitude0
ClinVar
Risk rs587779097(T;T)
Alt rs587779097(T;T)
Reference rs587779097(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47693814C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076189.2,