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rs745664511

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs745664511(A;G)
Make rs745664511(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position166051892
GeneSCN1A
is asnp
is mentioned by
dbSNPrs745664511
ebirs745664511
HLIrs745664511
Exacrs745664511
Varsomers745664511
Maprs745664511
PheGenIrs745664511
hapmaprs745664511
1000 genomesrs745664511
hgdprs745664511
ensemblrs745664511
gopubmedrs745664511
geneviewrs745664511
scholarrs745664511
googlers745664511
pharmgkbrs745664511
gwascentralrs745664511
openSNPrs745664511
23andMers745664511
23andMe allrs745664511
SNP Nexus

SNPshotrs745664511
SNPdbers745664511
MSV3drs745664511
GWAS Ctlgrs745664511
Max Magnitude0
ClinVar
Risk rs745664511(G;G)
Alt rs745664511(G;G)
Reference rs745664511(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166908402A>G
CLNSRC
CLNACC RCV000188847.2,