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rs1064797368

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position46853765
GeneRP2
is asnp
is mentioned by
dbSNPrs1064797368
dbSNP (old)rs1064797368
ClinGenrs1064797368
ebirs1064797368
HLIrs1064797368
Exacrs1064797368
Gnomadrs1064797368
Varsomers1064797368
Maprs1064797368
PheGenIrs1064797368
Biobankrs1064797368
1000 genomesrs1064797368
hgdprs1064797368
ensemblrs1064797368
gopubmedrs1064797368
geneviewrs1064797368
scholarrs1064797368
googlers1064797368
pharmgkbrs1064797368
gwascentralrs1064797368
openSNPrs1064797368
23andMers1064797368
23andMe allrs1064797368
SNPshotrs1064797368
SNPdbers1064797368
MSV3drs1064797368
GWAS Ctlgrs1064797368
Max Magnitude0
ClinVar
Risk rs1064797368(-;-)
Alt rs1064797368(-;-)
Reference Rs1064797368(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RP2
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.46713200delG
CLNSRC
CLNACC RCV000487802.1,