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rs587779251

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779251(-;-)
Make rs587779251(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800959
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779251
ebirs587779251
HLIrs587779251
Exacrs587779251
Varsomers587779251
Maprs587779251
PheGenIrs587779251
hapmaprs587779251
1000 genomesrs587779251
hgdprs587779251
ensemblrs587779251
gopubmedrs587779251
geneviewrs587779251
scholarrs587779251
googlers587779251
pharmgkbrs587779251
gwascentralrs587779251
openSNPrs587779251
23andMers587779251
23andMe allrs587779251
SNP Nexus

SNPshotrs587779251
SNPdbers587779251
MSV3drs587779251
GWAS Ctlgrs587779251
Max Magnitude0
ClinVar
Risk rs587779251(;)
Alt rs587779251(;)
Reference rs587779251(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48028098delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074791.2,