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rs1064797364

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position38286112
GeneRPGR
is asnp
is mentioned by
dbSNPrs1064797364
dbSNP (old)rs1064797364
ClinGenrs1064797364
ebirs1064797364
HLIrs1064797364
Exacrs1064797364
Gnomadrs1064797364
Varsomers1064797364
Maprs1064797364
PheGenIrs1064797364
Biobankrs1064797364
1000 genomesrs1064797364
hgdprs1064797364
ensemblrs1064797364
gopubmedrs1064797364
geneviewrs1064797364
scholarrs1064797364
googlers1064797364
pharmgkbrs1064797364
gwascentralrs1064797364
openSNPrs1064797364
23andMers1064797364
23andMe allrs1064797364
SNPshotrs1064797364
SNPdbers1064797364
MSV3drs1064797364
GWAS Ctlgrs1064797364
Max Magnitude0
ClinVar
Risk rs1064797364(-;-)
Alt rs1064797364(-;-)
Reference Rs1064797364(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RPGR
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.38145365delC
CLNSRC
CLNACC RCV000487721.1,