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rs71539659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs71539659(-;-)
Make rs71539659(-;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position47799852
GeneMSH6
is asnp
is mentioned by
dbSNPrs71539659
ebirs71539659
HLIrs71539659
Exacrs71539659
Varsomers71539659
Maprs71539659
PheGenIrs71539659
hapmaprs71539659
1000 genomesrs71539659
hgdprs71539659
ensemblrs71539659
gopubmedrs71539659
geneviewrs71539659
scholarrs71539659
googlers71539659
pharmgkbrs71539659
gwascentralrs71539659
openSNPrs71539659
23andMers71539659
23andMe allrs71539659
SNP Nexus

SNPshotrs71539659
SNPdbers71539659
MSV3drs71539659
GWAS Ctlgrs71539659
Max Magnitude0
ClinVar
Risk rs71539659(;)
Alt rs71539659(;)
Reference rs71539659(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026991delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074694.2,