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rs587776706

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776706(-;-)
Make rs587776706(-;T)
Make rs587776706(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position47805694
GeneMSH6
is asnp
is mentioned by
dbSNPrs587776706
ebirs587776706
HLIrs587776706
Exacrs587776706
Varsomers587776706
Maprs587776706
PheGenIrs587776706
hapmaprs587776706
1000 genomesrs587776706
hgdprs587776706
ensemblrs587776706
gopubmedrs587776706
geneviewrs587776706
scholarrs587776706
googlers587776706
pharmgkbrs587776706
gwascentralrs587776706
openSNPrs587776706
23andMers587776706
23andMe allrs587776706
SNP Nexus

SNPshotrs587776706
SNPdbers587776706
MSV3drs587776706
GWAS Ctlgrs587776706
Max Magnitude0
ClinVar
Risk rs587776706(T;T)
Alt rs587776706(T;T)
Reference rs587776706(;)
Significance Pathogenic
Disease Turcot syndrome
Variation info
Gene MSH6
CLNDBN Turcot syndrome
Reversed 0
HGVS NC_000002.11:g.48032833dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000009497.5,