rs1057520743

Orientation

plus

Stabilized

plus

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

Make rs1057520743(C;G)

Make rs1057520743(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

147128829

Gene

CNTNAP2

is a	snp
is	mentioned by
dbSNP	rs1057520743
dbSNP (classic)	rs1057520743
ClinGen	rs1057520743
ebi	rs1057520743
HLI	rs1057520743
Exac	rs1057520743
Gnomad	rs1057520743
Varsome	rs1057520743
LitVar	rs1057520743
Map	rs1057520743
PheGenI	rs1057520743
Biobank	rs1057520743
1000 genomes	rs1057520743
hgdp	rs1057520743
ensembl	rs1057520743
geneview	rs1057520743
scholar	rs1057520743
google	rs1057520743
pharmgkb	rs1057520743
gwascentral	rs1057520743
openSNP	rs1057520743
23andMe	rs1057520743
SNPshot	rs1057520743
SNPdbe	rs1057520743
MSV3d	rs1057520743
GWAS Ctlg	rs1057520743

Max Magnitude

0

ClinVar
Risk	rs1057520743(G;G)
Alt	rs1057520743(G;G)
Reference	Rs1057520743(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CNTNAP2
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.146825921C>G
CLNSRC
CLNACC	RCV000421673.1,