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rs1064796071

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Chromosome7
Position147395761
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs1064796071
dbSNP (old)rs1064796071
ClinGenrs1064796071
ebirs1064796071
HLIrs1064796071
Exacrs1064796071
Gnomadrs1064796071
Varsomers1064796071
Maprs1064796071
PheGenIrs1064796071
Biobankrs1064796071
1000 genomesrs1064796071
hgdprs1064796071
ensemblrs1064796071
gopubmedrs1064796071
geneviewrs1064796071
scholarrs1064796071
googlers1064796071
pharmgkbrs1064796071
gwascentralrs1064796071
openSNPrs1064796071
23andMers1064796071
23andMe allrs1064796071
SNPshotrs1064796071
SNPdbers1064796071
MSV3drs1064796071
GWAS Ctlgrs1064796071
Max Magnitude0
ClinVar
Risk rs1064796071(-;-)
Alt rs1064796071(-;-)
Reference Rs1064796071(AT;AT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CNTNAP2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.147092853_147092854delAT
CLNSRC
CLNACC RCV000482314.1,