rs61751386

Orientation

minus

Stabilized

minus

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

Make rs61751386(-;-)

Make rs61751386(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

94062667

Gene

ABCA4

is a	snp
is	mentioned by
dbSNP	rs61751386
dbSNP (classic)	rs61751386
ClinGen	rs61751386
ebi	rs61751386
HLI	rs61751386
Exac	rs61751386
Gnomad	rs61751386
Varsome	rs61751386
LitVar	rs61751386
Map	rs61751386
PheGenI	rs61751386
Biobank	rs61751386
1000 genomes	rs61751386
hgdp	rs61751386
ensembl	rs61751386
geneview	rs61751386
scholar	rs61751386
google	rs61751386
pharmgkb	rs61751386
gwascentral	rs61751386
openSNP	rs61751386
23andMe	rs61751386
SNPshot	rs61751386
SNPdbe	rs61751386
MSV3d	rs61751386
GWAS Ctlg	rs61751386

Merged from

Rs387906386

Max Magnitude

0

ClinVar
Risk	rs61751386(-;-)
Alt	rs61751386(-;-)
Reference	Rs61751386(A;A)
Significance	Pathogenic
Disease	Retinitis pigmentosa 19 not provided
Variation	info
Gene	ABCA4
CLNDBN	Retinitis pigmentosa 19 not provided
Reversed	1
HGVS	NC_000001.10:g.94528222delT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008342.3, RCV000085435.1,