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rs587779241

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779241(-;-)
Make rs587779241(-;T)
Make rs587779241(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800518
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779241
ebirs587779241
HLIrs587779241
Exacrs587779241
Varsomers587779241
Maprs587779241
PheGenIrs587779241
hapmaprs587779241
1000 genomesrs587779241
hgdprs587779241
ensemblrs587779241
gopubmedrs587779241
geneviewrs587779241
scholarrs587779241
googlers587779241
pharmgkbrs587779241
gwascentralrs587779241
openSNPrs587779241
23andMers587779241
23andMe allrs587779241
SNP Nexus

SNPshotrs587779241
SNPdbers587779241
MSV3drs587779241
GWAS Ctlgrs587779241
Max Magnitude0
ClinVar
Risk rs587779241(T;T)
Alt rs587779241(T;T)
Reference rs587779241(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027657dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074751.2,