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rs1064797365

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position38286653
GeneRPGR
is asnp
is mentioned by
dbSNPrs1064797365
dbSNP (old)rs1064797365
ClinGenrs1064797365
ebirs1064797365
HLIrs1064797365
Exacrs1064797365
Gnomadrs1064797365
Varsomers1064797365
Maprs1064797365
PheGenIrs1064797365
Biobankrs1064797365
1000 genomesrs1064797365
hgdprs1064797365
ensemblrs1064797365
gopubmedrs1064797365
geneviewrs1064797365
scholarrs1064797365
googlers1064797365
pharmgkbrs1064797365
gwascentralrs1064797365
openSNPrs1064797365
23andMers1064797365
23andMe allrs1064797365
SNPshotrs1064797365
SNPdbers1064797365
MSV3drs1064797365
GWAS Ctlgrs1064797365
Max Magnitude0
ClinVar
Risk rs1064797365(-;-)
Alt rs1064797365(-;-)
Reference Rs1064797365(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RPGR
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.38145906delC
CLNSRC
CLNACC RCV000488008.1,