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

rs1057518062

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518062(A;T)
Make rs1057518062(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166002476
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1057518062
dbSNP (old)rs1057518062
ClinGenrs1057518062
ebirs1057518062
HLIrs1057518062
Exacrs1057518062
Gnomadrs1057518062
Varsomers1057518062
LitVarrs1057518062
Maprs1057518062
PheGenIrs1057518062
Biobankrs1057518062
1000 genomesrs1057518062
hgdprs1057518062
ensemblrs1057518062
gopubmedrs1057518062
geneviewrs1057518062
scholarrs1057518062
googlers1057518062
pharmgkbrs1057518062
gwascentralrs1057518062
openSNPrs1057518062
23andMers1057518062
23andMe allrs1057518062
SNPshotrs1057518062
SNPdbers1057518062
MSV3drs1057518062
GWAS Ctlgrs1057518062
Max Magnitude0
ClinVar
Risk rs1057518062(T;T)
Alt rs1057518062(T;T)
Reference Rs1057518062(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166858986T>A
CLNSRC
CLNACC RCV000414265.1,