Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057519236

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519236(G;T)
Make rs1057519236(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position38286214
GeneRPGR
is asnp
is mentioned by
dbSNPrs1057519236
dbSNP (old)rs1057519236
ClinGenrs1057519236
ebirs1057519236
HLIrs1057519236
Exacrs1057519236
Gnomadrs1057519236
Varsomers1057519236
Maprs1057519236
PheGenIrs1057519236
Biobankrs1057519236
1000 genomesrs1057519236
hgdprs1057519236
ensemblrs1057519236
gopubmedrs1057519236
geneviewrs1057519236
scholarrs1057519236
googlers1057519236
pharmgkbrs1057519236
gwascentralrs1057519236
openSNPrs1057519236
23andMers1057519236
23andMe allrs1057519236
SNPshotrs1057519236
SNPdbers1057519236
MSV3drs1057519236
GWAS Ctlgrs1057519236
Max Magnitude0
ClinVar
Risk rs1057519236(T;T)
Alt rs1057519236(T;T)
Reference Rs1057519236(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RPGR
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.38145467C>A
CLNSRC
CLNACC RCV000415877.1,