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rs794729207

From SNPedia

Orientationminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs794729207(-;-)
Make rs794729207(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166036520
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs794729207
ebirs794729207
HLIrs794729207
Exacrs794729207
Varsomers794729207
Maprs794729207
PheGenIrs794729207
hapmaprs794729207
1000 genomesrs794729207
hgdprs794729207
ensemblrs794729207
gopubmedrs794729207
geneviewrs794729207
scholarrs794729207
googlers794729207
pharmgkbrs794729207
gwascentralrs794729207
openSNPrs794729207
23andMers794729207
23andMe allrs794729207
SNP Nexus

SNPshotrs794729207
SNPdbers794729207
MSV3drs794729207
GWAS Ctlgrs794729207
Max Magnitude0
ClinVar
Risk rs794729207(;)
Alt rs794729207(;)
Reference rs794729207(CT;CT)
Significance Pathogenic
Disease Generalized epilepsy with febrile seizures plus
Variation info
Gene LOC102724058 SCN1A
CLNDBN Generalized epilepsy with febrile seizures plus, type 2
Reversed 1
HGVS NC_000002.11:g.166893030_166893031delAG
CLNSRC
CLNACC RCV000184026.1,