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rs1057518658

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs1057518658(-;-)
Make rs1057518658(-;AC)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165331409
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057518658
dbSNP (old)rs1057518658
ClinGenrs1057518658
ebirs1057518658
HLIrs1057518658
Exacrs1057518658
Gnomadrs1057518658
Varsomers1057518658
Maprs1057518658
PheGenIrs1057518658
Biobankrs1057518658
1000 genomesrs1057518658
hgdprs1057518658
ensemblrs1057518658
gopubmedrs1057518658
geneviewrs1057518658
scholarrs1057518658
googlers1057518658
pharmgkbrs1057518658
gwascentralrs1057518658
openSNPrs1057518658
23andMers1057518658
23andMe allrs1057518658
SNPshotrs1057518658
SNPdbers1057518658
MSV3drs1057518658
GWAS Ctlgrs1057518658
Max Magnitude0
ClinVar
Risk rs1057518658(-;-)
Alt rs1057518658(-;-)
Reference Rs1057518658(AC;AC)
Significance Pathogenic
Disease Autism
Variation info
Gene SCN2A
CLNDBN Autism
Reversed 0
HGVS NC_000002.11:g.166187919_166187920delAC
CLNSRC
CLNACC RCV000414894.1,