rs762135776

Orientation

plus

Stabilized

plus

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

Make rs762135776(A;G)

Make rs762135776(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

42885815

Gene

PTPRT

is a	snp
is	mentioned by
dbSNP	rs762135776
dbSNP (classic)	rs762135776
ClinGen	rs762135776
ebi	rs762135776
HLI	rs762135776
Exac	rs762135776
Gnomad	rs762135776
Varsome	rs762135776
LitVar	rs762135776
Map	rs762135776
PheGenI	rs762135776
Biobank	rs762135776
1000 genomes	rs762135776
hgdp	rs762135776
ensembl	rs762135776
geneview	rs762135776
scholar	rs762135776
google	rs762135776
pharmgkb	rs762135776
gwascentral	rs762135776
openSNP	rs762135776
23andMe	rs762135776
SNPshot	rs762135776
SNPdbe	rs762135776
MSV3d	rs762135776
GWAS Ctlg	rs762135776

Max Magnitude

0

ClinVar
Risk	rs762135776(G;G)
Alt	rs762135776(G;G)
Reference	Rs762135776(A;A)
Significance	Probable-Pathogenic
Disease	Abnormality of brain morphology
Variation	info
Gene	PTPRT
CLNDBN	Abnormality of brain morphology
Reversed	0
HGVS	NC_000020.10:g.41514455A>G
CLNSRC
CLNACC	RCV000454261.1,