rs796052374

Orientation

plus

Stabilized

plus

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

Make rs796052374(C;G)

Make rs796052374(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

147132507

Gene

CNTNAP2

is a	snp
is	mentioned by
dbSNP	rs796052374
dbSNP (classic)	rs796052374
ClinGen	rs796052374
ebi	rs796052374
HLI	rs796052374
Exac	rs796052374
Gnomad	rs796052374
Varsome	rs796052374
LitVar	rs796052374
Map	rs796052374
PheGenI	rs796052374
Biobank	rs796052374
1000 genomes	rs796052374
hgdp	rs796052374
ensembl	rs796052374
geneview	rs796052374
scholar	rs796052374
google	rs796052374
pharmgkb	rs796052374
gwascentral	rs796052374
openSNP	rs796052374
23andMe	rs796052374
SNPshot	rs796052374
SNPdbe	rs796052374
MSV3d	rs796052374
GWAS Ctlg	rs796052374

Max Magnitude

0

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,