rs273585629

Orientation

plus

Stabilized

plus

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

Make rs273585629(A;A)

Make rs273585629(A;G)

Reference

GRCh38 38.1/142

Chromosome

16

Position

88438655

Gene

ZNF469

is a	snp
is	mentioned by
dbSNP	rs273585629
dbSNP (classic)	rs273585629
ClinGen	rs273585629
ebi	rs273585629
HLI	rs273585629
Exac	rs273585629
Gnomad	rs273585629
Varsome	rs273585629
LitVar	rs273585629
Map	rs273585629
PheGenI	rs273585629
Biobank	rs273585629
1000 genomes	rs273585629
hgdp	rs273585629
ensembl	rs273585629
geneview	rs273585629
scholar	rs273585629
google	rs273585629
pharmgkb	rs273585629
gwascentral	rs273585629
openSNP	rs273585629
23andMe	rs273585629
SNPshot	rs273585629
SNPdbe	rs273585629
MSV3d	rs273585629
GWAS Ctlg	rs273585629

Max Magnitude

0

ClinVar
Risk	rs273585629(A;A)
Alt	rs273585629(A;A)
Reference	Rs273585629(G;G)
Significance	Pathogenic
Disease	Keratoconus 1
Variation	info
Gene	ZNF469
CLNDBN	Keratoconus 1
Reversed	0
HGVS	NC_000016.9:g.88505063G>A
CLNSRC	ClinVar
CLNACC	RCV000114774.1,