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rs786203924

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs786203924(-;-)
Make rs786203924(-;AT)
Make rs786203924(AT;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47800889
GeneMSH6
is asnp
is mentioned by
dbSNPrs786203924
ebirs786203924
HLIrs786203924
Exacrs786203924
Varsomers786203924
Maprs786203924
PheGenIrs786203924
hapmaprs786203924
1000 genomesrs786203924
hgdprs786203924
ensemblrs786203924
gopubmedrs786203924
geneviewrs786203924
scholarrs786203924
googlers786203924
pharmgkbrs786203924
gwascentralrs786203924
openSNPrs786203924
23andMers786203924
23andMe allrs786203924
SNP Nexus

SNPshotrs786203924
SNPdbers786203924
MSV3drs786203924
GWAS Ctlgrs786203924
Max Magnitude0
ClinVar
Risk rs786203924(;)
Alt rs786203924(;)
Reference rs786203924(TA;TA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48028028_48028029delAT
CLNSRC
CLNACC RCV000167441.1,