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rs786201043

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786201043(-;-)
Make rs786201043(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47796014
GeneMSH6
is asnp
is mentioned by
dbSNPrs786201043
ebirs786201043
HLIrs786201043
Exacrs786201043
Varsomers786201043
Maprs786201043
PheGenIrs786201043
hapmaprs786201043
1000 genomesrs786201043
hgdprs786201043
ensemblrs786201043
gopubmedrs786201043
geneviewrs786201043
scholarrs786201043
googlers786201043
pharmgkbrs786201043
gwascentralrs786201043
openSNPrs786201043
23andMers786201043
23andMe allrs786201043
SNP Nexus

SNPshotrs786201043
SNPdbers786201043
MSV3drs786201043
GWAS Ctlgrs786201043
Max Magnitude0
ClinVar
Risk rs786201043(;)
Alt rs786201043(;)
Reference rs786201043(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48023153delT
CLNSRC
CLNACC RCV000162426.2, RCV000231303.1,