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rs2286455

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2286455(A;A)
Make rs2286455(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position16018539
GenePROM1
is asnp
is mentioned by
dbSNPrs2286455
dbSNP (old)rs2286455
ClinGenrs2286455
ebirs2286455
HLIrs2286455
Exacrs2286455
Varsomers2286455
Maprs2286455
PheGenIrs2286455
Biobankrs2286455
1000 genomesrs2286455
hgdprs2286455
ensemblrs2286455
gopubmedrs2286455
geneviewrs2286455
scholarrs2286455
googlers2286455
pharmgkbrs2286455
gwascentralrs2286455
openSNPrs2286455
23andMers2286455
23andMe allrs2286455
SNP Nexus

SNPshotrs2286455
SNPdbers2286455
MSV3drs2286455
GWAS Ctlgrs2286455
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 26406410] Association of CD133 polymorphisms and response to bevacizumab in patients with metastatic colorectal cancer


ClinVar
Risk rs2286455(A;A)
Alt rs2286455(A;A)
Reference Rs2286455(G;G)
Significance Probable-non-pathogenic
Disease not specified Cone-Rod Dystrophy Retinitis Pigmentosa Stargardt Disease Retinal Macular Dystrophy
Variation info
Gene PROM1
CLNDBN not specified Cone-Rod Dystrophy, Dominant Retinitis Pigmentosa, Recessive Stargardt Disease, Dominant Retinal Macular Dystrophy
Reversed 1
HGVS NC_000004.11:g.16020162C>T
CLNSRC
CLNACC RCV000250373.1, RCV000279196.1, RCV000336486.1, RCV000375986.1, RCV000379416.1,