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rs875989778

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989778(C;C)
Make rs875989778(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position13479429
GeneRAB28
is asnp
is mentioned by
dbSNPrs875989778
ebirs875989778
HLIrs875989778
Exacrs875989778
Varsomers875989778
Maprs875989778
PheGenIrs875989778
hapmaprs875989778
1000 genomesrs875989778
hgdprs875989778
ensemblrs875989778
gopubmedrs875989778
geneviewrs875989778
scholarrs875989778
googlers875989778
pharmgkbrs875989778
gwascentralrs875989778
openSNPrs875989778
23andMers875989778
23andMe allrs875989778
SNP Nexus

SNPshotrs875989778
SNPdbers875989778
MSV3drs875989778
GWAS Ctlgrs875989778
Max Magnitude0
ClinVar
Risk rs875989778(C;C)
Alt rs875989778(C;C)
Reference rs875989778(G;G)
Significance Pathogenic
Disease Cone-rod dystrophy 18
Variation info
Gene RAB28
CLNDBN Cone-rod dystrophy 18
Reversed 1
HGVS NC_000004.11:g.13481053C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000211098.2,