rs796052388

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs796052388(-;-)

Make rs796052388(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

147121075

Gene

CNTNAP2

is a	snp
is	mentioned by
dbSNP	rs796052388
dbSNP (classic)	rs796052388
ClinGen	rs796052388
ebi	rs796052388
HLI	rs796052388
Exac	rs796052388
Gnomad	rs796052388
Varsome	rs796052388
LitVar	rs796052388
Map	rs796052388
PheGenI	rs796052388
Biobank	rs796052388
1000 genomes	rs796052388
hgdp	rs796052388
ensembl	rs796052388
geneview	rs796052388
scholar	rs796052388
google	rs796052388
pharmgkb	rs796052388
gwascentral	rs796052388
openSNP	rs796052388
23andMe	rs796052388
SNPshot	rs796052388
SNPdbe	rs796052388
MSV3d	rs796052388
GWAS Ctlg	rs796052388

Max Magnitude

0

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,