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rs1064793317

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome20
Position63406708
GeneKCNQ2
is asnp
is mentioned by
dbSNPrs1064793317
dbSNP (classic)rs1064793317
ClinGenrs1064793317
ebirs1064793317
HLIrs1064793317
Exacrs1064793317
Gnomadrs1064793317
Varsomers1064793317
LitVarrs1064793317
Maprs1064793317
PheGenIrs1064793317
Biobankrs1064793317
1000 genomesrs1064793317
hgdprs1064793317
ensemblrs1064793317
geneviewrs1064793317
scholarrs1064793317
googlers1064793317
pharmgkbrs1064793317
gwascentralrs1064793317
openSNPrs1064793317
23andMers1064793317
23andMe allrs1064793317
SNPshotrs1064793317
SNPdbers1064793317
MSV3drs1064793317
GWAS Ctlgrs1064793317
Max Magnitude0
ClinVar
Risk rs1064793317(-;-)
Alt rs1064793317(-;-)
Reference Rs1064793317(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNQ2
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.62038061delG
CLNSRC
CLNACC RCV000480144.1,