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rs786205259

From SNPedia

Orientationminus
Geno Mag Summary
(TTTG;TTTG) 0 common in clinvar
Make rs786205259(-;-)
Make rs786205259(-;TTTG)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position73322592
GeneHCN4
is asnp
is mentioned by
dbSNPrs786205259
ebirs786205259
HLIrs786205259
Exacrs786205259
Varsomers786205259
Maprs786205259
PheGenIrs786205259
hapmaprs786205259
1000 genomesrs786205259
hgdprs786205259
ensemblrs786205259
gopubmedrs786205259
geneviewrs786205259
scholarrs786205259
googlers786205259
pharmgkbrs786205259
gwascentralrs786205259
openSNPrs786205259
23andMers786205259
23andMe allrs786205259
SNP Nexus

SNPshotrs786205259
SNPdbers786205259
MSV3drs786205259
GWAS Ctlgrs786205259
Max Magnitude0
ClinVar
Risk rs786205259(;)
Alt rs786205259(;)
Reference rs786205259(TTTG;TTTG)
Significance Probable-Pathogenic
Disease Sinus node disease
Variation info
Gene HCN4
CLNDBN Sinus node disease
Reversed 1
HGVS NC_000015.9:g.73614933_73614936delCAAA
CLNSRC
CLNACC RCV000171563.1,