rs1060499749

Orientation

minus

Stabilized

minus

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

Make rs1060499749(C;T)

Make rs1060499749(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

42352288

Gene

PTPRT

is a	snp
is	mentioned by
dbSNP	rs1060499749
dbSNP (classic)	rs1060499749
ClinGen	rs1060499749
ebi	rs1060499749
HLI	rs1060499749
Exac	rs1060499749
Gnomad	rs1060499749
Varsome	rs1060499749
LitVar	rs1060499749
Map	rs1060499749
PheGenI	rs1060499749
Biobank	rs1060499749
1000 genomes	rs1060499749
hgdp	rs1060499749
ensembl	rs1060499749
geneview	rs1060499749
scholar	rs1060499749
google	rs1060499749
pharmgkb	rs1060499749
gwascentral	rs1060499749
openSNP	rs1060499749
23andMe	rs1060499749
SNPshot	rs1060499749
SNPdbe	rs1060499749
MSV3d	rs1060499749
GWAS Ctlg	rs1060499749

Max Magnitude

0

ClinVar
Risk	rs1060499749(T;T)
Alt	rs1060499749(T;T)
Reference	Rs1060499749(C;C)
Significance	Probable-Pathogenic
Disease	Abnormality of brain morphology
Variation	info
Gene	PTPRT
CLNDBN	Abnormality of brain morphology
Reversed	1
HGVS	NC_000020.10:g.40980928G>A
CLNSRC
CLNACC	RCV000454175.1,