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rs587779260

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779260(-;-)
Make rs587779260(-;C)
Make rs587779260(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47803588
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779260
ebirs587779260
HLIrs587779260
Exacrs587779260
Varsomers587779260
Maprs587779260
PheGenIrs587779260
hapmaprs587779260
1000 genomesrs587779260
hgdprs587779260
ensemblrs587779260
gopubmedrs587779260
geneviewrs587779260
scholarrs587779260
googlers587779260
pharmgkbrs587779260
gwascentralrs587779260
openSNPrs587779260
23andMers587779260
23andMe allrs587779260
SNP Nexus

SNPshotrs587779260
SNPdbers587779260
MSV3drs587779260
GWAS Ctlgrs587779260
Max Magnitude0
ClinVar
Risk rs587779260(C;C)
Alt rs587779260(C;C)
Reference rs587779260(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030727_48030728insC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074841.2,