rs398124268

Orientation

plus

Stabilized

plus

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

Make rs398124268(A;A)

Make rs398124268(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

147903619

Gene

CNTNAP2

is a	snp
is	mentioned by
dbSNP	rs398124268
dbSNP (classic)	rs398124268
ClinGen	rs398124268
ebi	rs398124268
HLI	rs398124268
Exac	rs398124268
Gnomad	rs398124268
Varsome	rs398124268
LitVar	rs398124268
Map	rs398124268
PheGenI	rs398124268
Biobank	rs398124268
1000 genomes	rs398124268
hgdp	rs398124268
ensembl	rs398124268
geneview	rs398124268
scholar	rs398124268
google	rs398124268
pharmgkb	rs398124268
gwascentral	rs398124268
openSNP	rs398124268
23andMe	rs398124268
SNPshot	rs398124268
SNPdbe	rs398124268
MSV3d	rs398124268
GWAS Ctlg	rs398124268

Max Magnitude

0

ClinVar
Risk	rs398124268(A;A)
Alt	rs398124268(A;A)
Reference	Rs398124268(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CNTNAP2
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.147600711G>A
CLNSRC	HGMD
CLNACC	RCV000081591.6,