Have questions? Visit https://www.reddit.com/r/SNPedia

rs587780455

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common genotype
Make rs587780455(A;G)
Make rs587780455(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome12
Position51807116
GeneSCN8A
is asnp
is mentioned by
dbSNPrs587780455
dbSNP (classic)rs587780455
ClinGenrs587780455
ebirs587780455
HLIrs587780455
Exacrs587780455
Gnomadrs587780455
Varsomers587780455
LitVarrs587780455
Maprs587780455
PheGenIrs587780455
Biobankrs587780455
1000 genomesrs587780455
hgdprs587780455
ensemblrs587780455
geneviewrs587780455
scholarrs587780455
googlers587780455
pharmgkbrs587780455
gwascentralrs587780455
openSNPrs587780455
23andMers587780455
23andMe allrs587780455
SNPshotrs587780455
SNPdbers587780455
MSV3drs587780455
GWAS Ctlgrs587780455
Max Magnitude0

aka NM_014191.3(SCN8A):c.5630A>G or (p.Asn1877Ser)

OMIM pathogenic variant