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rs794727128

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794727128(A;G)
Make rs794727128(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position51751510
GeneSCN8A
is asnp
is mentioned by
dbSNPrs794727128
dbSNP (classic)rs794727128
ClinGenrs794727128
ebirs794727128
HLIrs794727128
Exacrs794727128
Gnomadrs794727128
Varsomers794727128
LitVarrs794727128
Maprs794727128
PheGenIrs794727128
Biobankrs794727128
1000 genomesrs794727128
hgdprs794727128
ensemblrs794727128
geneviewrs794727128
scholarrs794727128
googlers794727128
pharmgkbrs794727128
gwascentralrs794727128
openSNPrs794727128
23andMers794727128
23andMe allrs794727128
SNPshotrs794727128
SNPdbers794727128
MSV3drs794727128
GWAS Ctlgrs794727128
Max Magnitude0
ClinVar
Risk rs794727128(G;G)
Alt rs794727128(G;G)
Reference Rs794727128(A;A)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene SCN8A
CLNDBN not provided not specified
Reversed 0
HGVS NC_000012.11:g.52145294A>G
CLNSRC
CLNACC RCV000174766.3, RCV000259124.1,