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rs786205418

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205418(-;-)
Make rs786205418(-;GTGA)
Make rs786205418(GTGA;GTGA)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position73343384
GeneHCN4, LOC105370890
is asnp
is mentioned by
dbSNPrs786205418
ebirs786205418
HLIrs786205418
Exacrs786205418
Varsomers786205418
Maprs786205418
PheGenIrs786205418
hapmaprs786205418
1000 genomesrs786205418
hgdprs786205418
ensemblrs786205418
gopubmedrs786205418
geneviewrs786205418
scholarrs786205418
googlers786205418
pharmgkbrs786205418
gwascentralrs786205418
openSNPrs786205418
23andMers786205418
23andMe allrs786205418
SNP Nexus

SNPshotrs786205418
SNPdbers786205418
MSV3drs786205418
GWAS Ctlgrs786205418
Max Magnitude0
ClinVar
Risk rs786205418(GAGT;GAGT)
Alt rs786205418(GAGT;GAGT)
Reference rs786205418(;)
Significance Pathogenic
Disease Brugada syndrome 8 Ventricular tachycardia
Variation info
Gene HCN4
CLNDBN Brugada syndrome 8 Ventricular tachycardia
Reversed 1
HGVS NC_000015.9:g.73635725_73635726insTCAC
CLNSRC OMIM Allelic Variant
CLNACC RCV000005485.3, RCV000171564.1,