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rs587777277

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777277(A;A)
Make rs587777277(A;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position93585358
GeneNR2F1
is asnp
is mentioned by
dbSNPrs587777277
ebirs587777277
HLIrs587777277
Exacrs587777277
Varsomers587777277
Maprs587777277
PheGenIrs587777277
hapmaprs587777277
1000 genomesrs587777277
hgdprs587777277
ensemblrs587777277
gopubmedrs587777277
geneviewrs587777277
scholarrs587777277
googlers587777277
pharmgkbrs587777277
gwascentralrs587777277
openSNPrs587777277
23andMers587777277
23andMe allrs587777277
SNP Nexus

SNPshotrs587777277
SNPdbers587777277
MSV3drs587777277
GWAS Ctlgrs587777277
Max Magnitude0
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
CLNACC RCV000114390.4,