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rs281865373

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281865373(A;T)
Make rs281865373(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position42704362
GenePRPH2
is asnp
is mentioned by
dbSNPrs281865373
ebirs281865373
HLIrs281865373
Exacrs281865373
Varsomers281865373
Maprs281865373
PheGenIrs281865373
hapmaprs281865373
1000 genomesrs281865373
hgdprs281865373
ensemblrs281865373
gopubmedrs281865373
geneviewrs281865373
scholarrs281865373
googlers281865373
pharmgkbrs281865373
gwascentralrs281865373
openSNPrs281865373
23andMers281865373
23andMe allrs281865373
SNP Nexus

SNPshotrs281865373
SNPdbers281865373
MSV3drs281865373
GWAS Ctlgrs281865373
Max Magnitude0
ClinVar
Risk rs281865373(T;T)
Alt rs281865373(T;T)
Reference rs281865373(A;A)
Significance Pathogenic
Disease not provided Retinitis pigmentosa 7
Variation info
Gene PRPH2
CLNDBN not provided Retinitis pigmentosa 7
Reversed 1
HGVS NC_000006.11:g.42672100T>A
CLNSRC
CLNACC RCV000085026.1, RCV000175582.1,