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rs1060499536

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499536(A;G)
Make rs1060499536(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position149896778
GenePDE6A
is asnp
is mentioned by
dbSNPrs1060499536
dbSNP (old)rs1060499536
ClinGenrs1060499536
ebirs1060499536
HLIrs1060499536
Exacrs1060499536
Gnomadrs1060499536
Varsomers1060499536
LitVarrs1060499536
Maprs1060499536
PheGenIrs1060499536
Biobankrs1060499536
1000 genomesrs1060499536
hgdprs1060499536
ensemblrs1060499536
gopubmedrs1060499536
geneviewrs1060499536
scholarrs1060499536
googlers1060499536
pharmgkbrs1060499536
gwascentralrs1060499536
openSNPrs1060499536
23andMers1060499536
23andMe allrs1060499536
SNPshotrs1060499536
SNPdbers1060499536
MSV3drs1060499536
GWAS Ctlgrs1060499536
Max Magnitude0
ClinVar
Risk rs1060499536(G;G)
Alt rs1060499536(G;G)
Reference Rs1060499536(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 43
Variation info
Gene PDE6A
CLNDBN Retinitis pigmentosa 43
Reversed 1
HGVS NC_000005.9:g.149276341T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000210743.1,