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rs1057524164

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524164(A;T)
Make rs1057524164(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165312082
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057524164
dbSNP (classic)rs1057524164
ClinGenrs1057524164
ebirs1057524164
HLIrs1057524164
Exacrs1057524164
Gnomadrs1057524164
Varsomers1057524164
LitVarrs1057524164
Maprs1057524164
PheGenIrs1057524164
Biobankrs1057524164
1000 genomesrs1057524164
hgdprs1057524164
ensemblrs1057524164
geneviewrs1057524164
scholarrs1057524164
googlers1057524164
pharmgkbrs1057524164
gwascentralrs1057524164
openSNPrs1057524164
23andMers1057524164
23andMe allrs1057524164
SNPshotrs1057524164
SNPdbers1057524164
MSV3drs1057524164
GWAS Ctlgrs1057524164
Max Magnitude0
ClinVar
Risk rs1057524164(T;T)
Alt rs1057524164(T;T)
Reference Rs1057524164(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166168592A>T
CLNSRC
CLNACC RCV000422511.1,