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

rs1057518258

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518258(A;A)
Make rs1057518258(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165992030
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1057518258
dbSNP (old)rs1057518258
ClinGenrs1057518258
ebirs1057518258
HLIrs1057518258
Exacrs1057518258
Gnomadrs1057518258
Varsomers1057518258
LitVarrs1057518258
Maprs1057518258
PheGenIrs1057518258
Biobankrs1057518258
1000 genomesrs1057518258
hgdprs1057518258
ensemblrs1057518258
gopubmedrs1057518258
geneviewrs1057518258
scholarrs1057518258
googlers1057518258
pharmgkbrs1057518258
gwascentralrs1057518258
openSNPrs1057518258
23andMers1057518258
23andMe allrs1057518258
SNPshotrs1057518258
SNPdbers1057518258
MSV3drs1057518258
GWAS Ctlgrs1057518258
Max Magnitude0
ClinVar
Risk rs1057518258(A;A)
Alt rs1057518258(A;A)
Reference Rs1057518258(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848540C>T
CLNSRC
CLNACC RCV000412769.1,