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rs1057520149

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520149(A;A)
Make rs1057520149(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position51790479
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1057520149
dbSNP (classic)rs1057520149
ClinGenrs1057520149
ebirs1057520149
HLIrs1057520149
Exacrs1057520149
Gnomadrs1057520149
Varsomers1057520149
LitVarrs1057520149
Maprs1057520149
PheGenIrs1057520149
Biobankrs1057520149
1000 genomesrs1057520149
hgdprs1057520149
ensemblrs1057520149
geneviewrs1057520149
scholarrs1057520149
googlers1057520149
pharmgkbrs1057520149
gwascentralrs1057520149
openSNPrs1057520149
23andMers1057520149
23andMe allrs1057520149
SNPshotrs1057520149
SNPdbers1057520149
MSV3drs1057520149
GWAS Ctlgrs1057520149
Max Magnitude0
ClinVar
Risk rs1057520149(A;A)
Alt rs1057520149(A;A)
Reference Rs1057520149(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52184263C>A
CLNSRC
CLNACC RCV000441856.1,