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rs786205867

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205867(A;A)
Make rs786205867(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position111787039
GeneKCND3, LOC105378905
is asnp
is mentioned by
dbSNPrs786205867
ebirs786205867
HLIrs786205867
Exacrs786205867
Varsomers786205867
Maprs786205867
PheGenIrs786205867
hapmaprs786205867
1000 genomesrs786205867
hgdprs786205867
ensemblrs786205867
gopubmedrs786205867
geneviewrs786205867
scholarrs786205867
googlers786205867
pharmgkbrs786205867
gwascentralrs786205867
openSNPrs786205867
23andMers786205867
23andMe allrs786205867
SNP Nexus

SNPshotrs786205867
SNPdbers786205867
MSV3drs786205867
GWAS Ctlgrs786205867
Max Magnitude0
ClinVar
Risk rs786205867(A;A)
Alt rs786205867(A;A)
Reference rs786205867(G;G)
Significance Pathogenic
Disease Brugada syndrome 9
Variation info
Gene KCND3
CLNDBN Brugada syndrome 9
Reversed 1
HGVS NC_000001.10:g.112329661C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000172844.2,