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rs1064793850

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTGGCAATTC;TTGGCAATTC) 0 common in clinvar
Chromosome2
Position165344614
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1064793850
dbSNP (classic)rs1064793850
ClinGenrs1064793850
ebirs1064793850
HLIrs1064793850
Exacrs1064793850
Gnomadrs1064793850
Varsomers1064793850
LitVarrs1064793850
Maprs1064793850
PheGenIrs1064793850
Biobankrs1064793850
1000 genomesrs1064793850
hgdprs1064793850
ensemblrs1064793850
geneviewrs1064793850
scholarrs1064793850
googlers1064793850
pharmgkbrs1064793850
gwascentralrs1064793850
openSNPrs1064793850
23andMers1064793850
SNPshotrs1064793850
SNPdbers1064793850
MSV3drs1064793850
GWAS Ctlgrs1064793850
Max Magnitude0
ClinVar
Risk rs1064793850(-;-)
Alt rs1064793850(-;-)
Reference Rs1064793850(TTGGCAATTC;TTGGCAATTC)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201124_166201133delTGGCAATTCT
CLNSRC
CLNACC RCV000480984.1,