rs587777277

Orientation

plus

Stabilized

plus

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

Make rs587777277(A;A)

Make rs587777277(A;G)

Reference

GRCh38 38.1/142

Chromosome

5

Position

93585358

Gene

NR2F1

is a	snp
is	mentioned by
dbSNP	rs587777277
dbSNP (classic)	rs587777277
ClinGen	rs587777277
ebi	rs587777277
HLI	rs587777277
Exac	rs587777277
Gnomad	rs587777277
Varsome	rs587777277
LitVar	rs587777277
Map	rs587777277
PheGenI	rs587777277
Biobank	rs587777277
1000 genomes	rs587777277
hgdp	rs587777277
ensembl	rs587777277
geneview	rs587777277
scholar	rs587777277
google	rs587777277
pharmgkb	rs587777277
gwascentral	rs587777277
openSNP	rs587777277
23andMe	rs587777277
SNPshot	rs587777277
SNPdbe	rs587777277
MSV3d	rs587777277
GWAS Ctlg	rs587777277

Max Magnitude

0

ClinVar
Risk	rs587777277(A;A)
Alt	rs587777277(A;A)
Reference	Rs587777277(G;G)
Significance	Other
Disease	Bosch-Boonstra-Schaaf optic atrophy syndrome
Variation	info
Gene	NR2F1
CLNDBN	Bosch-Boonstra-Schaaf optic atrophy syndrome
Reversed	0
HGVS	NC_000005.9:g.92921064G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000114390.4,