rs1064796071

Orientation

plus

Stabilized

plus

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

Chromosome

7

Position

147395761

Gene

CNTNAP2

is a	snp
is	mentioned by
dbSNP	rs1064796071
dbSNP (classic)	rs1064796071
ClinGen	rs1064796071
ebi	rs1064796071
HLI	rs1064796071
Exac	rs1064796071
Gnomad	rs1064796071
Varsome	rs1064796071
LitVar	rs1064796071
Map	rs1064796071
PheGenI	rs1064796071
Biobank	rs1064796071
1000 genomes	rs1064796071
hgdp	rs1064796071
ensembl	rs1064796071
geneview	rs1064796071
scholar	rs1064796071
google	rs1064796071
pharmgkb	rs1064796071
gwascentral	rs1064796071
openSNP	rs1064796071
23andMe	rs1064796071
SNPshot	rs1064796071
SNPdbe	rs1064796071
MSV3d	rs1064796071
GWAS Ctlg	rs1064796071

Max Magnitude

0

ClinVar
Risk	rs1064796071(-;-)
Alt	rs1064796071(-;-)
Reference	Rs1064796071(AT;AT)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CNTNAP2
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.147092853_147092854delAT
CLNSRC
CLNACC	RCV000482314.1,