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rs1057521662

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521662(C;C)
Make rs1057521662(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position51766016
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1057521662
dbSNP (old)rs1057521662
ClinGenrs1057521662
ebirs1057521662
HLIrs1057521662
Exacrs1057521662
Gnomadrs1057521662
Varsomers1057521662
Maprs1057521662
PheGenIrs1057521662
Biobankrs1057521662
1000 genomesrs1057521662
hgdprs1057521662
ensemblrs1057521662
gopubmedrs1057521662
geneviewrs1057521662
scholarrs1057521662
googlers1057521662
pharmgkbrs1057521662
gwascentralrs1057521662
openSNPrs1057521662
23andMers1057521662
23andMe allrs1057521662
SNPshotrs1057521662
SNPdbers1057521662
MSV3drs1057521662
GWAS Ctlgrs1057521662
Max Magnitude0
ClinVar
Risk rs1057521662(C;C)
Alt rs1057521662(C;C)
Reference Rs1057521662(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52159800G>C
CLNSRC
CLNACC RCV000439821.1,