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rs587777276

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777276(C;C)
Make rs587777276(C;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position93588208
GeneNR2F1
is asnp
is mentioned by
dbSNPrs587777276
ClinGenrs587777276
ebirs587777276
HLIrs587777276
Exacrs587777276
Varsomers587777276
Maprs587777276
PheGenIrs587777276
hapmaprs587777276
1000 genomesrs587777276
hgdprs587777276
ensemblrs587777276
gopubmedrs587777276
geneviewrs587777276
scholarrs587777276
googlers587777276
pharmgkbrs587777276
gwascentralrs587777276
openSNPrs587777276
23andMers587777276
23andMe allrs587777276
SNP Nexus

SNPshotrs587777276
SNPdbers587777276
MSV3drs587777276
GWAS Ctlgrs587777276
Max Magnitude0
ClinVar
Risk rs587777276(C;C)
Alt rs587777276(C;C)
Reference Rs587777276(T;T)
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.92923914T>C
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000114389.4,