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rs62641689

From SNPedia

Orientationplus
Stabilizedplus
Make rs62641689(C;C)
Make rs62641689(C;T)
Make rs62641689(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome15
Position73323818
GeneHCN4
is asnp
is mentioned by
dbSNPrs62641689
dbSNP (classic)rs62641689
ClinGenrs62641689
ebirs62641689
HLIrs62641689
Exacrs62641689
Gnomadrs62641689
Varsomers62641689
LitVarrs62641689
Maprs62641689
PheGenIrs62641689
Biobankrs62641689
1000 genomesrs62641689
hgdprs62641689
ensemblrs62641689
geneviewrs62641689
scholarrs62641689
googlers62641689
pharmgkbrs62641689
gwascentralrs62641689
openSNPrs62641689
23andMers62641689
SNPshotrs62641689
SNPdbers62641689
MSV3drs62641689
GWAS Ctlgrs62641689
Max Magnitude0
ClinVar
Risk rs62641689(A;A) rs62641689(T;T)
Alt rs62641689(A;A) rs62641689(T;T)
Reference rs62641689(C;C)
Significance Other
Disease not provided not specified Sudden cardiac death Brugada syndrome 8
Variation info
Gene HCN4
CLNDBN not provided not specified Sudden cardiac death Brugada syndrome 8
Reversed 0
HGVS NC_000015.9:g.73616159C>T
CLNSRC
CLNACC RCV000170931.5, RCV000185511.4, RCV000204998.1, RCV000230980.2,