rs104886478

Orientation

minus

Stabilized

minus

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

Make rs104886478(C;T)

Make rs104886478(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

151181233

Gene

ASB10

is a	snp
is	mentioned by
dbSNP	rs104886478
dbSNP (classic)	rs104886478
ClinGen	rs104886478
ebi	rs104886478
HLI	rs104886478
Exac	rs104886478
Gnomad	rs104886478
Varsome	rs104886478
LitVar	rs104886478
Map	rs104886478
PheGenI	rs104886478
Biobank	rs104886478
1000 genomes	rs104886478
hgdp	rs104886478
ensembl	rs104886478
geneview	rs104886478
scholar	rs104886478
google	rs104886478
pharmgkb	rs104886478
gwascentral	rs104886478
openSNP	rs104886478
23andMe	rs104886478
SNPshot	rs104886478
SNPdbe	rs104886478
MSV3d	rs104886478
GWAS Ctlg	rs104886478

GMAF

0.0004591

Max Magnitude

0

ClinVar
Risk	rs104886478(T;T)
Alt	rs104886478(T;T)
Reference	Rs104886478(C;C)
Significance	Pathogenic
Disease	Glaucoma 1
Variation	info
Gene	ASB10
CLNDBN	Glaucoma 1, open angle, F
Reversed	1
HGVS	NC_000007.13:g.150878320G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043656.3,

[PMID 10037570] GLC1F, a new primary open-angle glaucoma locus, maps to 7q35-q36.