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rs1064797215

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome17
Position1650839
GenePRPF8, RILP
is asnp
is mentioned by
dbSNPrs1064797215
dbSNP (classic)rs1064797215
ClinGenrs1064797215
ebirs1064797215
HLIrs1064797215
Exacrs1064797215
Gnomadrs1064797215
Varsomers1064797215
LitVarrs1064797215
Maprs1064797215
PheGenIrs1064797215
Biobankrs1064797215
1000 genomesrs1064797215
hgdprs1064797215
ensemblrs1064797215
geneviewrs1064797215
scholarrs1064797215
googlers1064797215
pharmgkbrs1064797215
gwascentralrs1064797215
openSNPrs1064797215
23andMers1064797215
SNPshotrs1064797215
SNPdbers1064797215
MSV3drs1064797215
GWAS Ctlgrs1064797215
Max Magnitude0
ClinVar
Risk rs1064797215(G;G)
Alt rs1064797215(G;G)
Reference Rs1064797215(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RILP PRPF8
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.1554134dup
CLNSRC
CLNACC RCV000487744.1,