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

rs1085307893

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position166002501
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1085307893
dbSNP (old)rs1085307893
ClinGenrs1085307893
ebirs1085307893
HLIrs1085307893
Exacrs1085307893
Gnomadrs1085307893
Varsomers1085307893
LitVarrs1085307893
Maprs1085307893
PheGenIrs1085307893
Biobankrs1085307893
1000 genomesrs1085307893
hgdprs1085307893
ensemblrs1085307893
gopubmedrs1085307893
geneviewrs1085307893
scholarrs1085307893
googlers1085307893
pharmgkbrs1085307893
gwascentralrs1085307893
openSNPrs1085307893
23andMers1085307893
23andMe allrs1085307893
SNPshotrs1085307893
SNPdbers1085307893
MSV3drs1085307893
GWAS Ctlgrs1085307893
Max Magnitude0
ClinVar
Risk rs1085307893(T;T)
Alt rs1085307893(T;T)
Reference Rs1085307893(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166859011C>A
CLNSRC
CLNACC RCV000489767.1,