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rs587779237

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs587779237(-;-)
Make rs587779237(-;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800362
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779237
ebirs587779237
HLIrs587779237
Exacrs587779237
Varsomers587779237
Maprs587779237
PheGenIrs587779237
hapmaprs587779237
1000 genomesrs587779237
hgdprs587779237
ensemblrs587779237
gopubmedrs587779237
geneviewrs587779237
scholarrs587779237
googlers587779237
pharmgkbrs587779237
gwascentralrs587779237
openSNPrs587779237
23andMers587779237
23andMe allrs587779237
SNP Nexus

SNPshotrs587779237
SNPdbers587779237
MSV3drs587779237
GWAS Ctlgrs587779237
Max Magnitude0
ClinVar
Risk rs587779237(;)
Alt rs587779237(;)
Reference rs587779237(TG;TG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027501_48027502delTG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074742.2,