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rs587779216

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779216(-;-)
Make rs587779216(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799573
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779216
ebirs587779216
HLIrs587779216
Exacrs587779216
Varsomers587779216
Maprs587779216
PheGenIrs587779216
hapmaprs587779216
1000 genomesrs587779216
hgdprs587779216
ensemblrs587779216
gopubmedrs587779216
geneviewrs587779216
scholarrs587779216
googlers587779216
pharmgkbrs587779216
gwascentralrs587779216
openSNPrs587779216
23andMers587779216
23andMe allrs587779216
SNP Nexus

SNPshotrs587779216
SNPdbers587779216
MSV3drs587779216
GWAS Ctlgrs587779216
Max Magnitude0
ClinVar
Risk rs587779216(;)
Alt rs587779216(;)
Reference rs587779216(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026712delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074667.2,