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rs587779289

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779289(-;-)
Make rs587779289(-;A)
Make rs587779289(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806314
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779289
ebirs587779289
HLIrs587779289
Exacrs587779289
Varsomers587779289
Maprs587779289
PheGenIrs587779289
hapmaprs587779289
1000 genomesrs587779289
hgdprs587779289
ensemblrs587779289
gopubmedrs587779289
geneviewrs587779289
scholarrs587779289
googlers587779289
pharmgkbrs587779289
gwascentralrs587779289
openSNPrs587779289
23andMers587779289
23andMe allrs587779289
SNP Nexus

SNPshotrs587779289
SNPdbers587779289
MSV3drs587779289
GWAS Ctlgrs587779289
Max Magnitude0
ClinVar
Risk rs587779289(A;A)
Alt rs587779289(A;A)
Reference rs587779289(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033453_48033454insA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074924.2,