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rs587779288

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779288(-;-)
Make rs587779288(-;ATTA)
Make rs587779288(ATTA;ATTA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47806289
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779288
ebirs587779288
HLIrs587779288
Exacrs587779288
Varsomers587779288
Maprs587779288
PheGenIrs587779288
hapmaprs587779288
1000 genomesrs587779288
hgdprs587779288
ensemblrs587779288
gopubmedrs587779288
geneviewrs587779288
scholarrs587779288
googlers587779288
pharmgkbrs587779288
gwascentralrs587779288
openSNPrs587779288
23andMers587779288
23andMe allrs587779288
SNP Nexus

SNPshotrs587779288
SNPdbers587779288
MSV3drs587779288
GWAS Ctlgrs587779288
Max Magnitude0
ClinVar
Risk rs587779288(ATTA;ATTA)
Alt rs587779288(ATTA;ATTA)
Reference rs587779288(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033425_48033428dupATTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074922.2,