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rs1057523393

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057523393(C;C)
Make rs1057523393(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position38556461
GeneSCN5A
is asnp
is mentioned by
dbSNPrs1057523393
dbSNP (old)rs1057523393
ClinGenrs1057523393
ebirs1057523393
HLIrs1057523393
Exacrs1057523393
Gnomadrs1057523393
Varsomers1057523393
Maprs1057523393
PheGenIrs1057523393
Biobankrs1057523393
1000 genomesrs1057523393
hgdprs1057523393
ensemblrs1057523393
gopubmedrs1057523393
geneviewrs1057523393
scholarrs1057523393
googlers1057523393
pharmgkbrs1057523393
gwascentralrs1057523393
openSNPrs1057523393
23andMers1057523393
23andMe allrs1057523393
SNPshotrs1057523393
SNPdbers1057523393
MSV3drs1057523393
GWAS Ctlgrs1057523393
Max Magnitude0
ClinVar
Risk rs1057523393(C;C)
Alt rs1057523393(C;C)
Reference Rs1057523393(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38597952A>G
CLNSRC
CLNACC RCV000424008.1,