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rs1064795784

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome3
Position38579477
GeneSCN5A
is asnp
is mentioned by
dbSNPrs1064795784
dbSNP (old)rs1064795784
ClinGenrs1064795784
ebirs1064795784
HLIrs1064795784
Exacrs1064795784
Gnomadrs1064795784
Varsomers1064795784
Maprs1064795784
PheGenIrs1064795784
Biobankrs1064795784
1000 genomesrs1064795784
hgdprs1064795784
ensemblrs1064795784
gopubmedrs1064795784
geneviewrs1064795784
scholarrs1064795784
googlers1064795784
pharmgkbrs1064795784
gwascentralrs1064795784
openSNPrs1064795784
23andMers1064795784
23andMe allrs1064795784
SNPshotrs1064795784
SNPdbers1064795784
MSV3drs1064795784
GWAS Ctlgrs1064795784
Max Magnitude0
ClinVar
Risk rs1064795784(-;-)
Alt rs1064795784(-;-)
Reference Rs1064795784(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38620968delA
CLNSRC
CLNACC RCV000480297.1,