rs17730281

Orientation

plus

Stabilized

plus

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

Make rs17730281(A;A)

Make rs17730281(A;G)

Reference

GRCh38 38.1/141

Chromosome

15

Position

53615751

Gene

WDR72

is a	snp
is	mentioned by
dbSNP	rs17730281
dbSNP (classic)	rs17730281
ClinGen	rs17730281
ebi	rs17730281
HLI	rs17730281
Exac	rs17730281
Gnomad	rs17730281
Varsome	rs17730281
LitVar	rs17730281
Map	rs17730281
PheGenI	rs17730281
Biobank	rs17730281
1000 genomes	rs17730281
hgdp	rs17730281
ensembl	rs17730281
geneview	rs17730281
scholar	rs17730281
google	rs17730281
pharmgkb	rs17730281
gwascentral	rs17730281
openSNP	rs17730281
23andMe	rs17730281
SNPshot	rs17730281
SNPdbe	rs17730281
MSV3d	rs17730281
GWAS Ctlg	rs17730281

GMAF

0.2801

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 22797727]
Trait	Renal function-related traits (BUN)
Title	Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.
Risk Allele	G
P-val	3E-11
Odds Ratio	.01 [0.0035-0.0067] mg/dl increase

ClinVar
Risk	rs17730281(A;A)
Alt	rs17730281(A;A)
Reference	Rs17730281(G;G)
Significance	Probable-non-pathogenic
Disease	not specified Amelogenesis Imperfecta
Variation	info
Gene	WDR72
CLNDBN	not specified Amelogenesis Imperfecta, Recessive
Reversed	0
HGVS	NC_000015.9:g.53907948G>A
CLNSRC
CLNACC	RCV000247021.1, RCV000271084.1,