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rs796052388

From SNPedia

Orientationplus
Make rs796052388(-;-)
Make rs796052388(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position147121075
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs796052388
ClinGenrs796052388
ebirs796052388
HLIrs796052388
Exacrs796052388
Varsomers796052388
Maprs796052388
PheGenIrs796052388
hapmaprs796052388
1000 genomesrs796052388
hgdprs796052388
ensemblrs796052388
gopubmedrs796052388
geneviewrs796052388
scholarrs796052388
googlers796052388
pharmgkbrs796052388
gwascentralrs796052388
openSNPrs796052388
23andMers796052388
23andMe allrs796052388
SNP Nexus

SNPshotrs796052388
SNPdbers796052388
MSV3drs796052388
GWAS Ctlgrs796052388
Max Magnitude
ClinVar
Risk
Alt
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,