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rs757532106

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757532106(A;A)
Make rs757532106(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38550500
GeneSCN5A
is asnp
is mentioned by
dbSNPrs757532106
ebirs757532106
HLIrs757532106
Exacrs757532106
Varsomers757532106
Maprs757532106
PheGenIrs757532106
hapmaprs757532106
1000 genomesrs757532106
hgdprs757532106
ensemblrs757532106
gopubmedrs757532106
geneviewrs757532106
scholarrs757532106
googlers757532106
pharmgkbrs757532106
gwascentralrs757532106
openSNPrs757532106
23andMers757532106
23andMe allrs757532106
SNP Nexus

SNPshotrs757532106
SNPdbers757532106
MSV3drs757532106
GWAS Ctlgrs757532106
Max Magnitude0
ClinVar
Risk rs757532106(A;A)
Alt rs757532106(A;A)
Reference rs757532106(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38591991G>A
CLNSRC
CLNACC RCV000183137.2,