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rs1057517958

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517958(C;T)
Make rs1057517958(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165991711
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1057517958
dbSNP (classic)rs1057517958
ClinGenrs1057517958
ebirs1057517958
HLIrs1057517958
Exacrs1057517958
Gnomadrs1057517958
Varsomers1057517958
LitVarrs1057517958
Maprs1057517958
PheGenIrs1057517958
Biobankrs1057517958
1000 genomesrs1057517958
hgdprs1057517958
ensemblrs1057517958
geneviewrs1057517958
scholarrs1057517958
googlers1057517958
pharmgkbrs1057517958
gwascentralrs1057517958
openSNPrs1057517958
23andMers1057517958
SNPshotrs1057517958
SNPdbers1057517958
MSV3drs1057517958
GWAS Ctlgrs1057517958
Max Magnitude0
ClinVar
Risk rs1057517958(T;T)
Alt rs1057517958(T;T)
Reference Rs1057517958(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848221G>A
CLNSRC
CLNACC RCV000414318.1,