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rs527236104

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs527236104(-;-)
Make rs527236104(-;G)
Make rs527236104(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position62613612
GeneEML3, ROM1
is asnp
is mentioned by
dbSNPrs527236104
ebirs527236104
HLIrs527236104
Exacrs527236104
Varsomers527236104
Maprs527236104
PheGenIrs527236104
hapmaprs527236104
1000 genomesrs527236104
hgdprs527236104
ensemblrs527236104
gopubmedrs527236104
geneviewrs527236104
scholarrs527236104
googlers527236104
pharmgkbrs527236104
gwascentralrs527236104
openSNPrs527236104
23andMers527236104
23andMe allrs527236104
SNP Nexus

SNPshotrs527236104
SNPdbers527236104
MSV3drs527236104
GWAS Ctlgrs527236104
Max Magnitude0
ClinVar
Risk rs527236104(G;G)
Alt rs527236104(G;G)
Reference rs527236104(;)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene EML3 ROM1
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000011.9:g.62381084dupG
CLNSRC ClinVar
CLNACC RCV000132581.1,