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rs797044507

From SNPedia

Orientationplus
Make rs797044507(-;-)
Make rs797044507(-;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position46853725
GeneRP2
is asnp
is mentioned by
dbSNPrs797044507
ebirs797044507
HLIrs797044507
Exacrs797044507
Varsomers797044507
Maprs797044507
PheGenIrs797044507
hapmaprs797044507
1000 genomesrs797044507
hgdprs797044507
ensemblrs797044507
gopubmedrs797044507
geneviewrs797044507
scholarrs797044507
googlers797044507
pharmgkbrs797044507
gwascentralrs797044507
openSNPrs797044507
23andMers797044507
23andMe allrs797044507
SNP Nexus

SNPshotrs797044507
SNPdbers797044507
MSV3drs797044507
GWAS Ctlgrs797044507
Max Magnitude
ClinVar
Risk rs797044507(;)
Alt rs797044507(;)
Reference rs797044507(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 2
Variation info
Gene RP2
CLNDBN Retinitis pigmentosa 2
Reversed 0
HGVS NC_000023.10:g.46713160delC
CLNSRC
CLNACC RCV000153853.3,