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rs587779259

From SNPedia

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Geno Mag Summary
(CTTAGAG;CTTAGAG) 0 common in clinvar
Make rs587779259(-;-)
Make rs587779259(-;GAGCTTA)
Make rs587779259(GAGCTTA;GAGCTTA)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47803515
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779259
ebirs587779259
HLIrs587779259
Exacrs587779259
Varsomers587779259
Maprs587779259
PheGenIrs587779259
hapmaprs587779259
1000 genomesrs587779259
hgdprs587779259
ensemblrs587779259
gopubmedrs587779259
geneviewrs587779259
scholarrs587779259
googlers587779259
pharmgkbrs587779259
gwascentralrs587779259
openSNPrs587779259
23andMers587779259
23andMe allrs587779259
SNP Nexus

SNPshotrs587779259
SNPdbers587779259
MSV3drs587779259
GWAS Ctlgrs587779259
Max Magnitude0
ClinVar
Risk rs587779259(;)
Alt rs587779259(;)
Reference rs587779259(CTTAGAG;CTTAGAG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030654_48030660delGAGCTTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074833.2,