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rs587779209

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779209(-;-)
Make rs587779209(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799259
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779209
ebirs587779209
HLIrs587779209
Exacrs587779209
Varsomers587779209
Maprs587779209
PheGenIrs587779209
hapmaprs587779209
1000 genomesrs587779209
hgdprs587779209
ensemblrs587779209
gopubmedrs587779209
geneviewrs587779209
scholarrs587779209
googlers587779209
pharmgkbrs587779209
gwascentralrs587779209
openSNPrs587779209
23andMers587779209
23andMe allrs587779209
SNP Nexus

SNPshotrs587779209
SNPdbers587779209
MSV3drs587779209
GWAS Ctlgrs587779209
Max Magnitude0
ClinVar
Risk rs587779209(;)
Alt rs587779209(;)
Reference rs587779209(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026398delT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074646.2,