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rs786201050

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786201050(-;-)
Make rs786201050(-;G)
Make rs786201050(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47800213
GeneMSH6
is asnp
is mentioned by
dbSNPrs786201050
ebirs786201050
HLIrs786201050
Exacrs786201050
Varsomers786201050
Maprs786201050
PheGenIrs786201050
hapmaprs786201050
1000 genomesrs786201050
hgdprs786201050
ensemblrs786201050
gopubmedrs786201050
geneviewrs786201050
scholarrs786201050
googlers786201050
pharmgkbrs786201050
gwascentralrs786201050
openSNPrs786201050
23andMers786201050
23andMe allrs786201050
SNP Nexus

SNPshotrs786201050
SNPdbers786201050
MSV3drs786201050
GWAS Ctlgrs786201050
Max Magnitude0
ClinVar
Risk rs786201050(G;G)
Alt rs786201050(G;G)
Reference rs786201050(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48027352dupG
CLNSRC
CLNACC RCV000162451.1, RCV000198617.2, RCV000221977.1,