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rs1064795388

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome8
Position143829279
GeneLOC107986985, NRBP2, PUF60
is asnp
is mentioned by
dbSNPrs1064795388
dbSNP (old)rs1064795388
ClinGenrs1064795388
ebirs1064795388
HLIrs1064795388
Exacrs1064795388
Gnomadrs1064795388
Varsomers1064795388
Maprs1064795388
PheGenIrs1064795388
Biobankrs1064795388
1000 genomesrs1064795388
hgdprs1064795388
ensemblrs1064795388
gopubmedrs1064795388
geneviewrs1064795388
scholarrs1064795388
googlers1064795388
pharmgkbrs1064795388
gwascentralrs1064795388
openSNPrs1064795388
23andMers1064795388
23andMe allrs1064795388
SNPshotrs1064795388
SNPdbers1064795388
MSV3drs1064795388
GWAS Ctlgrs1064795388
Max Magnitude0
ClinVar
Risk rs1064795388(A;A)
Alt rs1064795388(A;A)
Reference Rs1064795388(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PUF60
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.144911449C>T
CLNSRC
CLNACC RCV000478219.1,