rs61753037

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	Carrier of a mutation for Stargardt disease

Make rs61753037(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

94007703

Gene

ABCA4

is a	snp
is	mentioned by
dbSNP	rs61753037
dbSNP (classic)	rs61753037
ClinGen	rs61753037
ebi	rs61753037
HLI	rs61753037
Exac	rs61753037
Gnomad	rs61753037
Varsome	rs61753037
LitVar	rs61753037
Map	rs61753037
PheGenI	rs61753037
Biobank	rs61753037
1000 genomes	rs61753037
hgdp	rs61753037
ensembl	rs61753037
geneview	rs61753037
scholar	rs61753037
google	rs61753037
pharmgkb	rs61753037
gwascentral	rs61753037
openSNP	rs61753037
23andMe	rs61753037
SNPshot	rs61753037
SNPdbe	rs61753037
MSV3d	rs61753037
GWAS Ctlg	rs61753037

Max Magnitude

3

ClinVar
Risk	rs61753037(T;T)
Alt	rs61753037(T;T)
Reference	Rs61753037(C;C)
Significance	Probable-Pathogenic
Disease	not provided Stargardt disease 1
Variation	info
Gene	ABCA4
CLNDBN	not provided Stargardt disease 1
Reversed	1
HGVS	NC_000001.10:g.94473259G>A
CLNSRC
CLNACC	RCV000085779.1, RCV000408461.1,