rs1057520549

Orientation

plus

Stabilized

plus

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

Make rs1057520549(C;T)

Make rs1057520549(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

147639258

Gene

CNTNAP2

is a	snp
is	mentioned by
dbSNP	rs1057520549
dbSNP (classic)	rs1057520549
ClinGen	rs1057520549
ebi	rs1057520549
HLI	rs1057520549
Exac	rs1057520549
Gnomad	rs1057520549
Varsome	rs1057520549
LitVar	rs1057520549
Map	rs1057520549
PheGenI	rs1057520549
Biobank	rs1057520549
1000 genomes	rs1057520549
hgdp	rs1057520549
ensembl	rs1057520549
geneview	rs1057520549
scholar	rs1057520549
google	rs1057520549
pharmgkb	rs1057520549
gwascentral	rs1057520549
openSNP	rs1057520549
23andMe	rs1057520549
SNPshot	rs1057520549
SNPdbe	rs1057520549
MSV3d	rs1057520549
GWAS Ctlg	rs1057520549

Max Magnitude

0

ClinVar
Risk	rs1057520549(T;T)
Alt	rs1057520549(T;T)
Reference	Rs1057520549(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CNTNAP2
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.147336350C>T
CLNSRC
CLNACC	RCV000423733.1,