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rs794726862

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794726862(A;A)
Make rs794726862(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position93600698
GeneRBP4
is asnp
is mentioned by
dbSNPrs794726862
ebirs794726862
HLIrs794726862
Exacrs794726862
Varsomers794726862
Maprs794726862
PheGenIrs794726862
hapmaprs794726862
1000 genomesrs794726862
hgdprs794726862
ensemblrs794726862
gopubmedrs794726862
geneviewrs794726862
scholarrs794726862
googlers794726862
pharmgkbrs794726862
gwascentralrs794726862
openSNPrs794726862
23andMers794726862
23andMe allrs794726862
SNP Nexus

SNPshotrs794726862
SNPdbers794726862
MSV3drs794726862
GWAS Ctlgrs794726862
Max Magnitude0
ClinVar
Risk rs794726862(A;A)
Alt rs794726862(A;A)
Reference rs794726862(G;G)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene RBP4
CLNDBN Microphthalmia, isolated, with coloboma 10
Reversed 1
HGVS NC_000010.10:g.95360455C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000173003.2,