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rs138799232

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138799232(C;T)
Make rs138799232(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position166042333
GeneSCN1A
is asnp
is mentioned by
dbSNPrs138799232
ebirs138799232
HLIrs138799232
Exacrs138799232
Varsomers138799232
Maprs138799232
PheGenIrs138799232
hapmaprs138799232
1000 genomesrs138799232
hgdprs138799232
ensemblrs138799232
gopubmedrs138799232
geneviewrs138799232
scholarrs138799232
googlers138799232
pharmgkbrs138799232
gwascentralrs138799232
openSNPrs138799232
23andMers138799232
23andMe allrs138799232
SNP Nexus

SNPshotrs138799232
SNPdbers138799232
MSV3drs138799232
GWAS Ctlgrs138799232
Max Magnitude0
ClinVar
Risk rs138799232(T;T)
Alt rs138799232(T;T)
Reference rs138799232(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166898843C>T
CLNSRC
CLNACC RCV000188887.1,