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rs869312664

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312664(A;A)
Make rs869312664(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position165386920
GeneSCN2A
is asnp
is mentioned by
dbSNPrs869312664
ebirs869312664
HLIrs869312664
Exacrs869312664
Varsomers869312664
Maprs869312664
PheGenIrs869312664
hapmaprs869312664
1000 genomesrs869312664
hgdprs869312664
ensemblrs869312664
gopubmedrs869312664
geneviewrs869312664
scholarrs869312664
googlers869312664
pharmgkbrs869312664
gwascentralrs869312664
openSNPrs869312664
23andMers869312664
23andMe allrs869312664
SNP Nexus

SNPshotrs869312664
SNPdbers869312664
MSV3drs869312664
GWAS Ctlgrs869312664
Max Magnitude0
ClinVar
Risk rs869312664(A;A)
Alt rs869312664(A;A)
Reference rs869312664(G;G)
Significance Pathogenic
Disease Early infantile epileptic encephalopathy 11
Variation info
Gene SCN2A
CLNDBN Early infantile epileptic encephalopathy 11
Reversed 0
HGVS NC_000002.11:g.166243430G>A
CLNSRC
CLNACC RCV000209946.1,