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rs796052388

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052388(-;-)
Make rs796052388(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position147121075
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs796052388
dbSNP (old)rs796052388
ClinGenrs796052388
ebirs796052388
HLIrs796052388
Exacrs796052388
Gnomadrs796052388
Varsomers796052388
Maprs796052388
PheGenIrs796052388
Biobankrs796052388
1000 genomesrs796052388
hgdprs796052388
ensemblrs796052388
gopubmedrs796052388
geneviewrs796052388
scholarrs796052388
googlers796052388
pharmgkbrs796052388
gwascentralrs796052388
openSNPrs796052388
23andMers796052388
23andMe allrs796052388
SNP Nexus

SNPshotrs796052388
SNPdbers796052388
MSV3drs796052388
GWAS Ctlgrs796052388
Max Magnitude0
ClinVar
Risk rs796052388(-;-)
Alt rs796052388(-;-)
Reference Rs796052388(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CNTNAP2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.146818167delA
CLNSRC
CLNACC RCV000187252.1,