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rs587779250

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779250(-;-)
Make rs587779250(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800928
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779250
ebirs587779250
HLIrs587779250
Exacrs587779250
Varsomers587779250
Maprs587779250
PheGenIrs587779250
hapmaprs587779250
1000 genomesrs587779250
hgdprs587779250
ensemblrs587779250
gopubmedrs587779250
geneviewrs587779250
scholarrs587779250
googlers587779250
pharmgkbrs587779250
gwascentralrs587779250
openSNPrs587779250
23andMers587779250
23andMe allrs587779250
SNP Nexus

SNPshotrs587779250
SNPdbers587779250
MSV3drs587779250
GWAS Ctlgrs587779250
Max Magnitude0
ClinVar
Risk rs587779250(;)
Alt rs587779250(;)
Reference rs587779250(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48028067delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074789.2,