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rs1085307838

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome7
Position148267031
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs1085307838
dbSNP (old)rs1085307838
ClinGenrs1085307838
ebirs1085307838
HLIrs1085307838
Exacrs1085307838
Gnomadrs1085307838
Varsomers1085307838
Maprs1085307838
PheGenIrs1085307838
Biobankrs1085307838
1000 genomesrs1085307838
hgdprs1085307838
ensemblrs1085307838
gopubmedrs1085307838
geneviewrs1085307838
scholarrs1085307838
googlers1085307838
pharmgkbrs1085307838
gwascentralrs1085307838
openSNPrs1085307838
23andMers1085307838
23andMe allrs1085307838
SNPshotrs1085307838
SNPdbers1085307838
MSV3drs1085307838
GWAS Ctlgrs1085307838
Max Magnitude0
ClinVar
Risk rs1085307838(C;C)
Alt rs1085307838(C;C)
Reference Rs1085307838(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CNTNAP2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.147964123A>C
CLNSRC
CLNACC RCV000489863.1,