rs1057518170

Orientation

minus

Stabilized

minus

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

Make rs1057518170(-;-)

Make rs1057518170(-;AT)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

151424959

Gene

POGZ

is a	snp
is	mentioned by
dbSNP	rs1057518170
dbSNP (classic)	rs1057518170
ClinGen	rs1057518170
ebi	rs1057518170
HLI	rs1057518170
Exac	rs1057518170
Gnomad	rs1057518170
Varsome	rs1057518170
LitVar	rs1057518170
Map	rs1057518170
PheGenI	rs1057518170
Biobank	rs1057518170
1000 genomes	rs1057518170
hgdp	rs1057518170
ensembl	rs1057518170
geneview	rs1057518170
scholar	rs1057518170
google	rs1057518170
pharmgkb	rs1057518170
gwascentral	rs1057518170
openSNP	rs1057518170
23andMe	rs1057518170
SNPshot	rs1057518170
SNPdbe	rs1057518170
MSV3d	rs1057518170
GWAS Ctlg	rs1057518170

Max Magnitude

0

ClinVar
Risk	rs1057518170(-;-)
Alt	rs1057518170(-;-)
Reference	Rs1057518170(AT;AT)
Significance	Pathogenic
Disease	not provided dysmorphy intellectual deficiency
Variation	info
Gene	POGZ
CLNDBN	not provided dysmorphy intellectual deficiency
Reversed	1
HGVS	NC_000001.10:g.151397435_151397436delAT
CLNSRC
CLNACC	RCV000414359.1, RCV000415179.1,