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rs797044735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044735(-;A)
Make rs797044735(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position54626582
GeneRP1
is asnp
is mentioned by
dbSNPrs797044735
dbSNP (old)rs797044735
ClinGenrs797044735
ebirs797044735
HLIrs797044735
Exacrs797044735
Gnomadrs797044735
Varsomers797044735
Maprs797044735
PheGenIrs797044735
Biobankrs797044735
1000 genomesrs797044735
hgdprs797044735
ensemblrs797044735
gopubmedrs797044735
geneviewrs797044735
scholarrs797044735
googlers797044735
pharmgkbrs797044735
gwascentralrs797044735
openSNPrs797044735
23andMers797044735
23andMe allrs797044735
SNP Nexus

SNPshotrs797044735
SNPdbers797044735
MSV3drs797044735
GWAS Ctlgrs797044735
Max Magnitude0
ClinVar
Risk rs797044735(A;A)
Alt rs797044735(A;A)
Reference Rs797044735(-;-)
Significance Pathogenic
Disease Retinitis pigmentosa 1 not provided
Variation info
Gene RP1
CLNDBN Retinitis pigmentosa 1 not provided
Reversed 0
HGVS NC_000008.10:g.55539142dupA
CLNSRC
CLNACC RCV000178263.1, RCV000488065.1,