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rs786205214

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205214(A;A)
Make rs786205214(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166041432
GeneSCN1A
is asnp
is mentioned by
dbSNPrs786205214
ebirs786205214
HLIrs786205214
Exacrs786205214
Varsomers786205214
Maprs786205214
PheGenIrs786205214
hapmaprs786205214
1000 genomesrs786205214
hgdprs786205214
ensemblrs786205214
gopubmedrs786205214
geneviewrs786205214
scholarrs786205214
googlers786205214
pharmgkbrs786205214
gwascentralrs786205214
openSNPrs786205214
23andMers786205214
23andMe allrs786205214
SNP Nexus

SNPshotrs786205214
SNPdbers786205214
MSV3drs786205214
GWAS Ctlgrs786205214
Max Magnitude0
ClinVar
Risk rs786205214(A;A)
Alt rs786205214(A;A)
Reference rs786205214(G;G)
Significance Pathogenic
Disease Generalized epilepsy with febrile seizures plus
Variation info
Gene SCN1A
CLNDBN Generalized epilepsy with febrile seizures plus, type 2
Reversed 1
HGVS NC_000002.11:g.166897942C>T
CLNSRC
CLNACC RCV000170444.1,