rs61732310

Orientation

minus

Stabilized

minus

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

Make rs61732310(C;T)

Make rs61732310(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

49061735

Gene

NTF4

is a	snp
is	mentioned by
dbSNP	rs61732310
dbSNP (classic)	rs61732310
ClinGen	rs61732310
ebi	rs61732310
HLI	rs61732310
Exac	rs61732310
Gnomad	rs61732310
Varsome	rs61732310
LitVar	rs61732310
Map	rs61732310
PheGenI	rs61732310
Biobank	rs61732310
1000 genomes	rs61732310
hgdp	rs61732310
ensembl	rs61732310
geneview	rs61732310
scholar	rs61732310
google	rs61732310
pharmgkb	rs61732310
gwascentral	rs61732310
openSNP	rs61732310
23andMe	rs61732310
SNPshot	rs61732310
SNPdbe	rs61732310
MSV3d	rs61732310
GWAS Ctlg	rs61732310

GMAF

0.001837

Max Magnitude

0

OMIM	162662
Desc
Variant	0001
Related	also

ClinVar
Risk	rs61732310(T;T)
Alt	rs61732310(T;T)
Reference	Rs61732310(C;C)
Significance	Pathogenic
Disease	Glaucoma 1
Variation	info
Gene	NTF4
CLNDBN	Glaucoma 1, open angle, O
Reversed	1
HGVS	NC_000019.9:g.49564992G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015060.25,