rs273585623

Orientation

plus

Stabilized

plus

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

Make rs273585623(A;A)

Make rs273585623(A;C)

Reference

GRCh38 38.1/142

Chromosome

16

Position

88433649

Gene

ZNF469

is a	snp
is	mentioned by
dbSNP	rs273585623
dbSNP (classic)	rs273585623
ClinGen	rs273585623
ebi	rs273585623
HLI	rs273585623
Exac	rs273585623
Gnomad	rs273585623
Varsome	rs273585623
LitVar	rs273585623
Map	rs273585623
PheGenI	rs273585623
Biobank	rs273585623
1000 genomes	rs273585623
hgdp	rs273585623
ensembl	rs273585623
geneview	rs273585623
scholar	rs273585623
google	rs273585623
pharmgkb	rs273585623
gwascentral	rs273585623
openSNP	rs273585623
23andMe	rs273585623
SNPshot	rs273585623
SNPdbe	rs273585623
MSV3d	rs273585623
GWAS Ctlg	rs273585623

Max Magnitude

0

ClinVar
Risk	rs273585623(A;A)
Alt	rs273585623(A;A)
Reference	Rs273585623(C;C)
Significance	Pathogenic
Disease	Keratoconus 1
Variation	info
Gene	ZNF469
CLNDBN	Keratoconus 1
Reversed	0
HGVS	NC_000016.9:g.88500057C>A
CLNSRC	ClinVar
CLNACC	RCV000114784.1,