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rs121918585

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918585(A;A)
Make rs121918585(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position93600470
GeneRBP4
is asnp
is mentioned by
dbSNPrs121918585
ebirs121918585
HLIrs121918585
Exacrs121918585
Varsomers121918585
Maprs121918585
PheGenIrs121918585
hapmaprs121918585
1000 genomesrs121918585
hgdprs121918585
ensemblrs121918585
gopubmedrs121918585
geneviewrs121918585
scholarrs121918585
googlers121918585
pharmgkbrs121918585
gwascentralrs121918585
openSNPrs121918585
23andMers121918585
23andMe allrs121918585
SNP Nexus

SNPshotrs121918585
SNPdbers121918585
MSV3drs121918585
GWAS Ctlgrs121918585
Max Magnitude0
OMIM180250
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121918585(A;A)
Alt rs121918585(A;A)
Reference rs121918585(G;G)
Significance Pathogenic
Disease Retinal dystrophy
Variation info
Gene RBP4
CLNDBN Retinal dystrophy, iris coloboma, and comedogenic acne syndrome
Reversed 1
HGVS NC_000010.10:g.95360227C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013943.26,