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rs794726861

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794726861(A;A)
Make rs794726861(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position93600692
GeneRBP4
is asnp
is mentioned by
dbSNPrs794726861
ClinGenrs794726861
ebirs794726861
HLIrs794726861
Exacrs794726861
Varsomers794726861
Maprs794726861
PheGenIrs794726861
hapmaprs794726861
1000 genomesrs794726861
hgdprs794726861
ensemblrs794726861
gopubmedrs794726861
geneviewrs794726861
scholarrs794726861
googlers794726861
pharmgkbrs794726861
gwascentralrs794726861
openSNPrs794726861
23andMers794726861
23andMe allrs794726861
SNP Nexus

SNPshotrs794726861
SNPdbers794726861
MSV3drs794726861
GWAS Ctlgrs794726861
Max Magnitude0
ClinVar
Risk rs794726861(A;A)
Alt rs794726861(A;A)
Reference Rs794726861(G;G)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene RBP4
CLNDBN Microphthalmia, isolated, with coloboma 10
Reversed 1
HGVS NC_000010.10:g.95360449C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000173002.2,