Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520486

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520486(A;A)
Make rs1057520486(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166037771
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1057520486
dbSNP (old)rs1057520486
ClinGenrs1057520486
ebirs1057520486
HLIrs1057520486
Exacrs1057520486
Gnomadrs1057520486
Varsomers1057520486
LitVarrs1057520486
Maprs1057520486
PheGenIrs1057520486
Biobankrs1057520486
1000 genomesrs1057520486
hgdprs1057520486
ensemblrs1057520486
gopubmedrs1057520486
geneviewrs1057520486
scholarrs1057520486
googlers1057520486
pharmgkbrs1057520486
gwascentralrs1057520486
openSNPrs1057520486
23andMers1057520486
23andMe allrs1057520486
SNPshotrs1057520486
SNPdbers1057520486
MSV3drs1057520486
GWAS Ctlgrs1057520486
Max Magnitude0
ClinVar
Risk rs1057520486(A;A)
Alt rs1057520486(A;A)
Reference Rs1057520486(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894281C>T
CLNSRC
CLNACC RCV000439519.1,