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rs786203597

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786203597(A;T)
Make rs786203597(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47796001
GeneMSH6
is asnp
is mentioned by
dbSNPrs786203597
ebirs786203597
HLIrs786203597
Exacrs786203597
Varsomers786203597
Maprs786203597
PheGenIrs786203597
hapmaprs786203597
1000 genomesrs786203597
hgdprs786203597
ensemblrs786203597
gopubmedrs786203597
geneviewrs786203597
scholarrs786203597
googlers786203597
pharmgkbrs786203597
gwascentralrs786203597
openSNPrs786203597
23andMers786203597
23andMe allrs786203597
SNP Nexus

SNPshotrs786203597
SNPdbers786203597
MSV3drs786203597
GWAS Ctlgrs786203597
Max Magnitude0
ClinVar
Risk rs786203597(T;T)
Alt rs786203597(T;T)
Reference rs786203597(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48023140A>T
CLNSRC
CLNACC RCV000166981.1,