rs869320712

Orientation

minus

Stabilized

minus

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

Make rs869320712(-;-)

Make rs869320712(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

15

Position

84643719

Gene

WDR73

is a	snp
is	mentioned by
dbSNP	rs869320712
dbSNP (classic)	rs869320712
ClinGen	rs869320712
ebi	rs869320712
HLI	rs869320712
Exac	rs869320712
Gnomad	rs869320712
Varsome	rs869320712
LitVar	rs869320712
Map	rs869320712
PheGenI	rs869320712
Biobank	rs869320712
1000 genomes	rs869320712
hgdp	rs869320712
ensembl	rs869320712
geneview	rs869320712
scholar	rs869320712
google	rs869320712
pharmgkb	rs869320712
gwascentral	rs869320712
openSNP	rs869320712
23andMe	rs869320712
SNPshot	rs869320712
SNPdbe	rs869320712
MSV3d	rs869320712
GWAS Ctlg	rs869320712

Max Magnitude

0

ClinVar
Risk	rs869320712(-;-)
Alt	rs869320712(-;-)
Reference	Rs869320712(T;T)
Significance	Pathogenic
Disease	Galloway-Mowat syndrome not provided
Variation	info
Gene	WDR73
CLNDBN	Galloway-Mowat syndrome not provided
Reversed	1
HGVS	NC_000015.9:g.85186950delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000210866.1, RCV000224128.1,