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rs200546024

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200546024(A;A)
Make rs200546024(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position73323571
GeneHCN4
is asnp
is mentioned by
dbSNPrs200546024
ebirs200546024
HLIrs200546024
Exacrs200546024
Varsomers200546024
Maprs200546024
PheGenIrs200546024
hapmaprs200546024
1000 genomesrs200546024
hgdprs200546024
ensemblrs200546024
gopubmedrs200546024
geneviewrs200546024
scholarrs200546024
googlers200546024
pharmgkbrs200546024
gwascentralrs200546024
openSNPrs200546024
23andMers200546024
23andMe allrs200546024
SNP Nexus

SNPshotrs200546024
SNPdbers200546024
MSV3drs200546024
GWAS Ctlgrs200546024
Max Magnitude0
ClinVar
Risk rs200546024(A;A)
Alt rs200546024(A;A)
Reference rs200546024(G;G)
Significance Other
Disease not provided Brugada syndrome 8
Variation info
Gene HCN4
CLNDBN not provided Brugada syndrome 8
Reversed 0
HGVS NC_000015.9:g.73615912G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000170941.4, RCV000223954.1,