Have questions? Visit https://www.reddit.com/r/SNPedia

rs727504075

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504075(A;A)
Make rs727504075(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position664945
GeneLOC102725200, PDE6B
is asnp
is mentioned by
dbSNPrs727504075
ebirs727504075
HLIrs727504075
Exacrs727504075
Varsomers727504075
Maprs727504075
PheGenIrs727504075
hapmaprs727504075
1000 genomesrs727504075
hgdprs727504075
ensemblrs727504075
gopubmedrs727504075
geneviewrs727504075
scholarrs727504075
googlers727504075
pharmgkbrs727504075
gwascentralrs727504075
openSNPrs727504075
23andMers727504075
23andMe allrs727504075
SNP Nexus

SNPshotrs727504075
SNPdbers727504075
MSV3drs727504075
GWAS Ctlgrs727504075
Max Magnitude0
ClinVar
Risk rs727504075(A;A)
Alt rs727504075(A;A)
Reference rs727504075(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 40 Retinitis pigmentosa
Variation info
Gene PDE6B LOC101928494
CLNDBN Retinitis pigmentosa 40 Retinitis pigmentosa
Reversed 0
HGVS NC_000004.11:g.658734G>A
CLNSRC HGMD
CLNACC RCV000153667.3, RCV000216602.1,