Have questions? Visit https://www.reddit.com/r/SNPedia

rs786202108

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786202108(-;-)
Make rs786202108(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47799755
GeneMSH6
is asnp
is mentioned by
dbSNPrs786202108
dbSNP (old)rs786202108
ClinGenrs786202108
ebirs786202108
HLIrs786202108
Exacrs786202108
Gnomadrs786202108
Varsomers786202108
Maprs786202108
PheGenIrs786202108
Biobankrs786202108
1000 genomesrs786202108
hgdprs786202108
ensemblrs786202108
gopubmedrs786202108
geneviewrs786202108
scholarrs786202108
googlers786202108
pharmgkbrs786202108
gwascentralrs786202108
openSNPrs786202108
23andMers786202108
23andMe allrs786202108
SNP Nexus

SNPshotrs786202108
SNPdbers786202108
MSV3drs786202108
GWAS Ctlgrs786202108
Max Magnitude0
ClinVar
Risk rs786202108(-;-)
Alt rs786202108(-;-)
Reference Rs786202108(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026894delC
CLNSRC
CLNACC RCV000164756.2,