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rs794728945

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs794728945(-;-)
Make rs794728945(-;ATCTG)
Make rs794728945(ATCTG;ATCTG)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position38554475
GeneSCN5A
is asnp
is mentioned by
dbSNPrs794728945
ebirs794728945
HLIrs794728945
Exacrs794728945
Varsomers794728945
Maprs794728945
PheGenIrs794728945
hapmaprs794728945
1000 genomesrs794728945
hgdprs794728945
ensemblrs794728945
gopubmedrs794728945
geneviewrs794728945
scholarrs794728945
googlers794728945
pharmgkbrs794728945
gwascentralrs794728945
openSNPrs794728945
23andMers794728945
23andMe allrs794728945
SNP Nexus

SNPshotrs794728945
SNPdbers794728945
MSV3drs794728945
GWAS Ctlgrs794728945
Max Magnitude0
ClinVar
Risk rs794728945(ATCTG;ATCTG)
Alt rs794728945(ATCTG;ATCTG)
Reference rs794728945(;)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.38595967_38595971dupCAGAT
CLNSRC
CLNACC RCV000183207.1,