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rs587776746

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AACA;AACA) 0 common in clinvar
Make rs587776746(-;-)
Make rs587776746(-;AACA)
ReferenceGRCh38 38.1/142
ChromosomeX
Position85878987
GeneCHM
is asnp
is mentioned by
dbSNPrs587776746
ebirs587776746
HLIrs587776746
Exacrs587776746
Varsomers587776746
Maprs587776746
PheGenIrs587776746
hapmaprs587776746
1000 genomesrs587776746
hgdprs587776746
ensemblrs587776746
gopubmedrs587776746
geneviewrs587776746
scholarrs587776746
googlers587776746
pharmgkbrs587776746
gwascentralrs587776746
openSNPrs587776746
23andMers587776746
23andMe allrs587776746
SNP Nexus

SNPshotrs587776746
SNPdbers587776746
MSV3drs587776746
GWAS Ctlgrs587776746
Max Magnitude0
ClinVar
Risk rs587776746(;)
Alt rs587776746(;)
Reference rs587776746(AACA;AACA)
Significance Pathogenic
Disease Choroideremia
Variation info
Gene CHM
CLNDBN Choroideremia
Reversed 0
HGVS NC_000023.10:g.85133992_85133995delAACA
CLNSRC OMIM Allelic Variant
CLNACC RCV000011902.7,