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rs587779217

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779217(-;-)
Make rs587779217(-;T)
Make rs587779217(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799579
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779217
ebirs587779217
HLIrs587779217
Exacrs587779217
Varsomers587779217
Maprs587779217
PheGenIrs587779217
hapmaprs587779217
1000 genomesrs587779217
hgdprs587779217
ensemblrs587779217
gopubmedrs587779217
geneviewrs587779217
scholarrs587779217
googlers587779217
pharmgkbrs587779217
gwascentralrs587779217
openSNPrs587779217
23andMers587779217
23andMe allrs587779217
SNP Nexus

SNPshotrs587779217
SNPdbers587779217
MSV3drs587779217
GWAS Ctlgrs587779217
Max Magnitude0
ClinVar
Risk rs587779217(T;T)
Alt rs587779217(T;T)
Reference rs587779217(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026718dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074668.2,