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rs769520392

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs769520392(A;G)
Make rs769520392(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position51706525
GeneSCN8A
is asnp
is mentioned by
dbSNPrs769520392
dbSNP (classic)rs769520392
ClinGenrs769520392
ebirs769520392
HLIrs769520392
Exacrs769520392
Gnomadrs769520392
Varsomers769520392
LitVarrs769520392
Maprs769520392
PheGenIrs769520392
Biobankrs769520392
1000 genomesrs769520392
hgdprs769520392
ensemblrs769520392
geneviewrs769520392
scholarrs769520392
googlers769520392
pharmgkbrs769520392
gwascentralrs769520392
openSNPrs769520392
23andMers769520392
23andMe allrs769520392
SNPshotrs769520392
SNPdbers769520392
MSV3drs769520392
GWAS Ctlgrs769520392
Max Magnitude0
ClinVar
Risk rs769520392(G;G)
Alt rs769520392(G;G)
Reference Rs769520392(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52100309A>G
CLNSRC
CLNACC RCV000434079.1,