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rs150401343

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150401343(A;A)
Make rs150401343(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position111780713
GeneKCND3
is asnp
is mentioned by
dbSNPrs150401343
dbSNP (old)rs150401343
ClinGenrs150401343
ebirs150401343
HLIrs150401343
Exacrs150401343
Gnomadrs150401343
Varsomers150401343
Maprs150401343
PheGenIrs150401343
Biobankrs150401343
1000 genomesrs150401343
hgdprs150401343
ensemblrs150401343
gopubmedrs150401343
geneviewrs150401343
scholarrs150401343
googlers150401343
pharmgkbrs150401343
gwascentralrs150401343
openSNPrs150401343
23andMers150401343
23andMe allrs150401343
SNP Nexus

SNPshotrs150401343
SNPdbers150401343
MSV3drs150401343
GWAS Ctlgrs150401343
Max Magnitude0
ClinVar
Risk rs150401343(A;A)
Alt rs150401343(A;A)
Reference Rs150401343(G;G)
Significance Pathogenic
Disease Brugada syndrome 9 not provided
Variation info
Gene KCND3
CLNDBN Brugada syndrome 9 not provided
Reversed 0
HGVS NC_000001.10:g.112323335G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000172842.3, RCV000415916.1,