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

rs1057518129

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518129(-;-)
Make rs1057518129(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166046769
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1057518129
dbSNP (old)rs1057518129
ClinGenrs1057518129
ebirs1057518129
HLIrs1057518129
Exacrs1057518129
Gnomadrs1057518129
Varsomers1057518129
Maprs1057518129
PheGenIrs1057518129
Biobankrs1057518129
1000 genomesrs1057518129
hgdprs1057518129
ensemblrs1057518129
gopubmedrs1057518129
geneviewrs1057518129
scholarrs1057518129
googlers1057518129
pharmgkbrs1057518129
gwascentralrs1057518129
openSNPrs1057518129
23andMers1057518129
23andMe allrs1057518129
SNPshotrs1057518129
SNPdbers1057518129
MSV3drs1057518129
GWAS Ctlgrs1057518129
Max Magnitude0
ClinVar
Risk rs1057518129(-;-)
Alt rs1057518129(-;-)
Reference Rs1057518129(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166903279delC
CLNSRC
CLNACC RCV000413091.1,