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rs775214722

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs775214722(A;G)
Make rs775214722(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position166037845
GeneSCN1A
is asnp
is mentioned by
dbSNPrs775214722
ebirs775214722
HLIrs775214722
Exacrs775214722
Varsomers775214722
Maprs775214722
PheGenIrs775214722
hapmaprs775214722
1000 genomesrs775214722
hgdprs775214722
ensemblrs775214722
gopubmedrs775214722
geneviewrs775214722
scholarrs775214722
googlers775214722
pharmgkbrs775214722
gwascentralrs775214722
openSNPrs775214722
23andMers775214722
23andMe allrs775214722
SNP Nexus

SNPshotrs775214722
SNPdbers775214722
MSV3drs775214722
GWAS Ctlgrs775214722
Max Magnitude0
ClinVar
Risk rs775214722(G,T;G,T)
Alt rs775214722(G,T;G,T)
Reference rs775214722(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166894355A>T
CLNSRC
CLNACC RCV000188901.1,