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rs786201084

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786201084(-;-)
Make rs786201084(-;T)
Make rs786201084(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47806300
GeneMSH6
is asnp
is mentioned by
dbSNPrs786201084
ebirs786201084
HLIrs786201084
Exacrs786201084
Varsomers786201084
Maprs786201084
PheGenIrs786201084
hapmaprs786201084
1000 genomesrs786201084
hgdprs786201084
ensemblrs786201084
gopubmedrs786201084
geneviewrs786201084
scholarrs786201084
googlers786201084
pharmgkbrs786201084
gwascentralrs786201084
openSNPrs786201084
23andMers786201084
23andMe allrs786201084
SNP Nexus

SNPshotrs786201084
SNPdbers786201084
MSV3drs786201084
GWAS Ctlgrs786201084
Max Magnitude0
ClinVar
Risk rs786201084(T;T)
Alt rs786201084(T;T)
Reference rs786201084(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48033439_48033440insT
CLNSRC
CLNACC RCV000162579.1,