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rs587779258

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779258(-;-)
Make rs587779258(-;T)
Make rs587779258(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47803506
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779258
ebirs587779258
HLIrs587779258
Exacrs587779258
Varsomers587779258
Maprs587779258
PheGenIrs587779258
hapmaprs587779258
1000 genomesrs587779258
hgdprs587779258
ensemblrs587779258
gopubmedrs587779258
geneviewrs587779258
scholarrs587779258
googlers587779258
pharmgkbrs587779258
gwascentralrs587779258
openSNPrs587779258
23andMers587779258
23andMe allrs587779258
SNP Nexus

SNPshotrs587779258
SNPdbers587779258
MSV3drs587779258
GWAS Ctlgrs587779258
Max Magnitude0
ClinVar
Risk rs587779258(T;T)
Alt rs587779258(T;T)
Reference rs587779258(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030645_48030646insT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074828.2,