rs387906386

Merged into

rs61751386

Orientation

minus

Stabilized

minus

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

Make rs387906386(-;-)

Make rs387906386(-;A)

Reference

GRCh38 38.1/141

Chromosome

1

Position

94062666

Gene

ABCA4

is a	snp
is	mentioned by
dbSNP	rs387906386
dbSNP (classic)	rs387906386
ClinGen	rs387906386
ebi	rs387906386
HLI	rs387906386
Exac	rs387906386
Gnomad	rs387906386
Varsome	rs387906386
LitVar	rs387906386
Map	rs387906386
PheGenI	rs387906386
Biobank	rs387906386
1000 genomes	rs387906386
hgdp	rs387906386
ensembl	rs387906386
geneview	rs387906386
scholar	rs387906386
google	rs387906386
pharmgkb	rs387906386
gwascentral	rs387906386
openSNP	rs387906386
23andMe	rs387906386
SNPshot	rs387906386
SNPdbe	rs387906386
MSV3d	rs387906386
GWAS Ctlg	rs387906386

Status

Merged into rs61751386

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs387906386(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,