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rs786203712

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786203712(-;-)
Make rs786203712(-;C)
Make rs786203712(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47803514
GeneMSH6
is asnp
is mentioned by
dbSNPrs786203712
ebirs786203712
HLIrs786203712
Exacrs786203712
Varsomers786203712
Maprs786203712
PheGenIrs786203712
hapmaprs786203712
1000 genomesrs786203712
hgdprs786203712
ensemblrs786203712
gopubmedrs786203712
geneviewrs786203712
scholarrs786203712
googlers786203712
pharmgkbrs786203712
gwascentralrs786203712
openSNPrs786203712
23andMers786203712
23andMe allrs786203712
SNP Nexus

SNPshotrs786203712
SNPdbers786203712
MSV3drs786203712
GWAS Ctlgrs786203712
Max Magnitude0
ClinVar
Risk rs786203712(C;C)
Alt rs786203712(C;C)
Reference rs786203712(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48030653_48030654insC
CLNSRC
CLNACC RCV000167133.1,