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rs1057518229

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518229(-;-)
Make rs1057518229(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166009823
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1057518229
dbSNP (old)rs1057518229
ClinGenrs1057518229
ebirs1057518229
HLIrs1057518229
Exacrs1057518229
Gnomadrs1057518229
Varsomers1057518229
Maprs1057518229
PheGenIrs1057518229
Biobankrs1057518229
1000 genomesrs1057518229
hgdprs1057518229
ensemblrs1057518229
gopubmedrs1057518229
geneviewrs1057518229
scholarrs1057518229
googlers1057518229
pharmgkbrs1057518229
gwascentralrs1057518229
openSNPrs1057518229
23andMers1057518229
23andMe allrs1057518229
SNPshotrs1057518229
SNPdbers1057518229
MSV3drs1057518229
GWAS Ctlgrs1057518229
Max Magnitude0
ClinVar
Risk rs1057518229(-;-)
Alt rs1057518229(-;-)
Reference Rs1057518229(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166866333delT
CLNSRC
CLNACC RCV000414152.1,