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rs111033578

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033578(C;G)
Make rs111033578(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position119339574
GeneC1QTNF5, MFRP
is asnp
is mentioned by
dbSNPrs111033578
ebirs111033578
HLIrs111033578
Exacrs111033578
Varsomers111033578
Maprs111033578
PheGenIrs111033578
hapmaprs111033578
1000 genomesrs111033578
hgdprs111033578
ensemblrs111033578
gopubmedrs111033578
geneviewrs111033578
scholarrs111033578
googlers111033578
pharmgkbrs111033578
gwascentralrs111033578
openSNPrs111033578
23andMers111033578
23andMe allrs111033578
SNP Nexus

SNPshotrs111033578
SNPdbers111033578
MSV3drs111033578
GWAS Ctlgrs111033578
Max Magnitude0
OMIM608752
Desc
Variant0001
Relatedalso
ClinVar
Risk rs111033578(G;G)
Alt rs111033578(G;G)
Reference rs111033578(C;C)
Significance Other
Disease Late-onset retinal degeneration
Variation info
Gene MFRP C1QTNF5
CLNDBN Late-onset retinal degeneration
Reversed 1
HGVS NC_000011.9:g.119210284G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002208.2,