rs752550849

Orientation

plus

Stabilized

plus

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

Make rs752550849(C;T)

Make rs752550849(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

147300239

Gene

CNTNAP2

is a	snp
is	mentioned by
dbSNP	rs752550849
dbSNP (classic)	rs752550849
ClinGen	rs752550849
ebi	rs752550849
HLI	rs752550849
Exac	rs752550849
Gnomad	rs752550849
Varsome	rs752550849
LitVar	rs752550849
Map	rs752550849
PheGenI	rs752550849
Biobank	rs752550849
1000 genomes	rs752550849
hgdp	rs752550849
ensembl	rs752550849
geneview	rs752550849
scholar	rs752550849
google	rs752550849
pharmgkb	rs752550849
gwascentral	rs752550849
openSNP	rs752550849
23andMe	rs752550849
SNPshot	rs752550849
SNPdbe	rs752550849
MSV3d	rs752550849
GWAS Ctlg	rs752550849

Max Magnitude

0

ClinVar
Risk	rs752550849(G;G) rs752550849(T;T)
Alt	rs752550849(G;G) rs752550849(T;T)
Reference	Rs752550849(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CNTNAP2
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.146997331C>T
CLNSRC
CLNACC	RCV000187185.1,