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rs1057517853

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517853(C;C)
Make rs1057517853(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165388667
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057517853
dbSNP (old)rs1057517853
ClinGenrs1057517853
ebirs1057517853
HLIrs1057517853
Exacrs1057517853
Gnomadrs1057517853
Varsomers1057517853
LitVarrs1057517853
Maprs1057517853
PheGenIrs1057517853
Biobankrs1057517853
1000 genomesrs1057517853
hgdprs1057517853
ensemblrs1057517853
gopubmedrs1057517853
geneviewrs1057517853
scholarrs1057517853
googlers1057517853
pharmgkbrs1057517853
gwascentralrs1057517853
openSNPrs1057517853
23andMers1057517853
23andMe allrs1057517853
SNPshotrs1057517853
SNPdbers1057517853
MSV3drs1057517853
GWAS Ctlgrs1057517853
Max Magnitude0
ClinVar
Risk rs1057517853(C;C)
Alt rs1057517853(C;C)
Reference Rs1057517853(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166245177T>C
CLNSRC
CLNACC RCV000414308.1,