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rs587779320

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779320(-;-)
Make rs587779320(-;T)
Make rs587779320(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47798721
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779320
ebirs587779320
HLIrs587779320
Exacrs587779320
Varsomers587779320
Maprs587779320
PheGenIrs587779320
hapmaprs587779320
1000 genomesrs587779320
hgdprs587779320
ensemblrs587779320
gopubmedrs587779320
geneviewrs587779320
scholarrs587779320
googlers587779320
pharmgkbrs587779320
gwascentralrs587779320
openSNPrs587779320
23andMers587779320
23andMe allrs587779320
SNP Nexus

SNPshotrs587779320
SNPdbers587779320
MSV3drs587779320
GWAS Ctlgrs587779320
Max Magnitude0
ClinVar
Risk rs587779320(T;T)
Alt rs587779320(T;T)
Reference rs587779320(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48025860_48025861insT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075030.2,