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rs1057517854

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517854(C;C)
Make rs1057517854(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165309386
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057517854
dbSNP (classic)rs1057517854
ClinGenrs1057517854
ebirs1057517854
HLIrs1057517854
Exacrs1057517854
Gnomadrs1057517854
Varsomers1057517854
LitVarrs1057517854
Maprs1057517854
PheGenIrs1057517854
Biobankrs1057517854
1000 genomesrs1057517854
hgdprs1057517854
ensemblrs1057517854
geneviewrs1057517854
scholarrs1057517854
googlers1057517854
pharmgkbrs1057517854
gwascentralrs1057517854
openSNPrs1057517854
23andMers1057517854
23andMe allrs1057517854
SNPshotrs1057517854
SNPdbers1057517854
MSV3drs1057517854
GWAS Ctlgrs1057517854
Max Magnitude0
ClinVar
Risk rs1057517854(C;C)
Alt rs1057517854(C;C)
Reference Rs1057517854(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166165896T>C
CLNSRC
CLNACC RCV000413157.1,