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rs786201052

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786201052(-;-)
Make rs786201052(-;G)
Make rs786201052(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47803663
GeneMSH6
is asnp
is mentioned by
dbSNPrs786201052
ebirs786201052
HLIrs786201052
Exacrs786201052
Varsomers786201052
Maprs786201052
PheGenIrs786201052
hapmaprs786201052
1000 genomesrs786201052
hgdprs786201052
ensemblrs786201052
gopubmedrs786201052
geneviewrs786201052
scholarrs786201052
googlers786201052
pharmgkbrs786201052
gwascentralrs786201052
openSNPrs786201052
23andMers786201052
23andMe allrs786201052
SNP Nexus

SNPshotrs786201052
SNPdbers786201052
MSV3drs786201052
GWAS Ctlgrs786201052
Max Magnitude0
ClinVar
Risk rs786201052(G;G)
Alt rs786201052(G;G)
Reference rs786201052(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48030802dupG
CLNSRC
CLNACC RCV000162454.1,