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rs1064796990

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position165991789
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1064796990
dbSNP (old)rs1064796990
ClinGenrs1064796990
ebirs1064796990
HLIrs1064796990
Exacrs1064796990
Gnomadrs1064796990
Varsomers1064796990
Maprs1064796990
PheGenIrs1064796990
Biobankrs1064796990
1000 genomesrs1064796990
hgdprs1064796990
ensemblrs1064796990
gopubmedrs1064796990
geneviewrs1064796990
scholarrs1064796990
googlers1064796990
pharmgkbrs1064796990
gwascentralrs1064796990
openSNPrs1064796990
23andMers1064796990
23andMe allrs1064796990
SNPshotrs1064796990
SNPdbers1064796990
MSV3drs1064796990
GWAS Ctlgrs1064796990
Max Magnitude0
ClinVar
Risk rs1064796990(-;-)
Alt rs1064796990(-;-)
Reference Rs1064796990(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848299delG
CLNSRC
CLNACC RCV000479294.1,