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rs1057521767

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521767(A;C)
Make rs1057521767(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position51789410
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1057521767
dbSNP (old)rs1057521767
ClinGenrs1057521767
ebirs1057521767
HLIrs1057521767
Exacrs1057521767
Gnomadrs1057521767
Varsomers1057521767
LitVarrs1057521767
Maprs1057521767
PheGenIrs1057521767
Biobankrs1057521767
1000 genomesrs1057521767
hgdprs1057521767
ensemblrs1057521767
gopubmedrs1057521767
geneviewrs1057521767
scholarrs1057521767
googlers1057521767
pharmgkbrs1057521767
gwascentralrs1057521767
openSNPrs1057521767
23andMers1057521767
23andMe allrs1057521767
SNPshotrs1057521767
SNPdbers1057521767
MSV3drs1057521767
GWAS Ctlgrs1057521767
Max Magnitude0
ClinVar
Risk rs1057521767(C;C)
Alt rs1057521767(C;C)
Reference Rs1057521767(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52183194A>C
CLNSRC
CLNACC RCV000438505.1,