Have questions? Visit https://www.reddit.com/r/SNPedia

rs863224903

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224903(C;C)
Make rs863224903(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position93585405
GeneNR2F1
is asnp
is mentioned by
dbSNPrs863224903
ebirs863224903
HLIrs863224903
Exacrs863224903
Varsomers863224903
Maprs863224903
PheGenIrs863224903
hapmaprs863224903
1000 genomesrs863224903
hgdprs863224903
ensemblrs863224903
gopubmedrs863224903
geneviewrs863224903
scholarrs863224903
googlers863224903
pharmgkbrs863224903
gwascentralrs863224903
openSNPrs863224903
23andMers863224903
23andMe allrs863224903
SNP Nexus

SNPshotrs863224903
SNPdbers863224903
MSV3drs863224903
GWAS Ctlgrs863224903
Max Magnitude0
ClinVar
Risk rs863224903(C;C)
Alt rs863224903(C;C)
Reference rs863224903(T;T)
Significance Probable-Pathogenic
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.92921111T>C
CLNSRC
CLNACC RCV000200428.1,