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rs112811136

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs112811136(C;G)
Make rs112811136(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position93600917
GeneRBP4
is asnp
is mentioned by
dbSNPrs112811136
ebirs112811136
HLIrs112811136
Exacrs112811136
Varsomers112811136
Maprs112811136
PheGenIrs112811136
hapmaprs112811136
1000 genomesrs112811136
hgdprs112811136
ensemblrs112811136
gopubmedrs112811136
geneviewrs112811136
scholarrs112811136
googlers112811136
pharmgkbrs112811136
gwascentralrs112811136
openSNPrs112811136
23andMers112811136
23andMe allrs112811136
SNP Nexus

SNPshotrs112811136
SNPdbers112811136
MSV3drs112811136
GWAS Ctlgrs112811136
Max Magnitude0
ClinVar
Risk rs112811136(A,G,T;A,G,T)
Alt rs112811136(A,G,T;A,G,T)
Reference rs112811136(C;C)
Significance Pathogenic
Disease Retinal dystrophy
Variation info
Gene RBP4
CLNDBN Retinal dystrophy, iris coloboma, and comedogenic acne syndrome
Reversed 0
HGVS NC_000010.10:g.95360674C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000034322.24,