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rs149344567

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs149344567(C;T)
Make rs149344567(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position111776247
GeneKCND3
is asnp
is mentioned by
dbSNPrs149344567
ebirs149344567
HLIrs149344567
Exacrs149344567
Varsomers149344567
Maprs149344567
PheGenIrs149344567
hapmaprs149344567
1000 genomesrs149344567
hgdprs149344567
ensemblrs149344567
gopubmedrs149344567
geneviewrs149344567
scholarrs149344567
googlers149344567
pharmgkbrs149344567
gwascentralrs149344567
openSNPrs149344567
23andMers149344567
23andMe allrs149344567
SNP Nexus

SNPshotrs149344567
SNPdbers149344567
MSV3drs149344567
GWAS Ctlgrs149344567
Max Magnitude0
ClinVar
Risk rs149344567(T;T)
Alt rs149344567(T;T)
Reference rs149344567(C;C)
Significance Pathogenic
Disease Brugada syndrome 9
Variation info
Gene KCND3
CLNDBN Brugada syndrome 9
Reversed 0
HGVS NC_000001.10:g.112318869C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000172843.2,