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rs786203968

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786203968(A;C)
Make rs786203968(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47804997
GeneMSH6
is asnp
is mentioned by
dbSNPrs786203968
ebirs786203968
HLIrs786203968
Exacrs786203968
Varsomers786203968
Maprs786203968
PheGenIrs786203968
hapmaprs786203968
1000 genomesrs786203968
hgdprs786203968
ensemblrs786203968
gopubmedrs786203968
geneviewrs786203968
scholarrs786203968
googlers786203968
pharmgkbrs786203968
gwascentralrs786203968
openSNPrs786203968
23andMers786203968
23andMe allrs786203968
SNP Nexus

SNPshotrs786203968
SNPdbers786203968
MSV3drs786203968
GWAS Ctlgrs786203968
Max Magnitude0
ClinVar
Risk rs786203968(C;C)
Alt rs786203968(C;C)
Reference rs786203968(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48032136A>C; NC_000002.11:g.48032136A>T
CLNSRC
CLNACC RCV000167501.1, RCV000204275.1,