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rs55958016

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs55958016(C;G)
Make rs55958016(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position216000489
GeneUSH2A
is asnp
is mentioned by
dbSNPrs55958016
ebirs55958016
HLIrs55958016
Exacrs55958016
Varsomers55958016
Maprs55958016
PheGenIrs55958016
hapmaprs55958016
1000 genomesrs55958016
hgdprs55958016
ensemblrs55958016
gopubmedrs55958016
geneviewrs55958016
scholarrs55958016
googlers55958016
pharmgkbrs55958016
gwascentralrs55958016
openSNPrs55958016
23andMers55958016
23andMe allrs55958016
SNP Nexus

SNPshotrs55958016
SNPdbers55958016
MSV3drs55958016
GWAS Ctlgrs55958016
Max Magnitude0
ClinVar
Risk rs55958016(A,G,T;A,G,T)
Alt rs55958016(A,G,T;A,G,T)
Reference rs55958016(C;C)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene USH2A
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000001.10:g.216173831C>T
CLNSRC ClinVar
CLNACC RCV000132714.1,