rs273585620

Orientation

plus

Stabilized

plus

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

Make rs273585620(G;T)

Make rs273585620(T;T)

Reference

GRCh38 38.1/142

Chromosome

16

Position

88431917

Gene

ZNF469

is a	snp
is	mentioned by
dbSNP	rs273585620
dbSNP (classic)	rs273585620
ClinGen	rs273585620
ebi	rs273585620
HLI	rs273585620
Exac	rs273585620
Gnomad	rs273585620
Varsome	rs273585620
LitVar	rs273585620
Map	rs273585620
PheGenI	rs273585620
Biobank	rs273585620
1000 genomes	rs273585620
hgdp	rs273585620
ensembl	rs273585620
geneview	rs273585620
scholar	rs273585620
google	rs273585620
pharmgkb	rs273585620
gwascentral	rs273585620
openSNP	rs273585620
23andMe	rs273585620
SNPshot	rs273585620
SNPdbe	rs273585620
MSV3d	rs273585620
GWAS Ctlg	rs273585620

Max Magnitude

0

ClinVar
Risk	rs273585620(A;A) rs273585620(T;T)
Alt	rs273585620(A;A) rs273585620(T;T)
Reference	Rs273585620(G;G)
Significance	Pathogenic
Disease	Keratoconus 1
Variation	info
Gene	ZNF469
CLNDBN	Keratoconus 1
Reversed	0
HGVS	NC_000016.9:g.88498325G>T
CLNSRC	ClinVar
CLNACC	RCV000114781.1,