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rs796052374

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052374(C;G)
Make rs796052374(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position147132507
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs796052374
ebirs796052374
HLIrs796052374
Exacrs796052374
Varsomers796052374
Maprs796052374
PheGenIrs796052374
hapmaprs796052374
1000 genomesrs796052374
hgdprs796052374
ensemblrs796052374
gopubmedrs796052374
geneviewrs796052374
scholarrs796052374
googlers796052374
pharmgkbrs796052374
gwascentralrs796052374
openSNPrs796052374
23andMers796052374
23andMe allrs796052374
SNP Nexus

SNPshotrs796052374
SNPdbers796052374
MSV3drs796052374
GWAS Ctlgrs796052374
Max Magnitude0
ClinVar
Risk rs796052374(G;G)
Alt rs796052374(G;G)
Reference rs796052374(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CNTNAP2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.146829599C>G
CLNSRC
CLNACC RCV000187182.1,