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rs1057518111

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518111(C;C)
Make rs1057518111(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165386974
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057518111
dbSNP (old)rs1057518111
ClinGenrs1057518111
ebirs1057518111
HLIrs1057518111
Exacrs1057518111
Gnomadrs1057518111
Varsomers1057518111
LitVarrs1057518111
Maprs1057518111
PheGenIrs1057518111
Biobankrs1057518111
1000 genomesrs1057518111
hgdprs1057518111
ensemblrs1057518111
gopubmedrs1057518111
geneviewrs1057518111
scholarrs1057518111
googlers1057518111
pharmgkbrs1057518111
gwascentralrs1057518111
openSNPrs1057518111
23andMers1057518111
23andMe allrs1057518111
SNPshotrs1057518111
SNPdbers1057518111
MSV3drs1057518111
GWAS Ctlgrs1057518111
Max Magnitude0
ClinVar
Risk rs1057518111(C;C)
Alt rs1057518111(C;C)
Reference Rs1057518111(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166243484T>C
CLNSRC
CLNACC RCV000414096.1,