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rs1064796360

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome3
Position180642123
GeneCCDC39
is asnp
is mentioned by
dbSNPrs1064796360
dbSNP (old)rs1064796360
ClinGenrs1064796360
ebirs1064796360
HLIrs1064796360
Exacrs1064796360
Gnomadrs1064796360
Varsomers1064796360
Maprs1064796360
PheGenIrs1064796360
Biobankrs1064796360
1000 genomesrs1064796360
hgdprs1064796360
ensemblrs1064796360
gopubmedrs1064796360
geneviewrs1064796360
scholarrs1064796360
googlers1064796360
pharmgkbrs1064796360
gwascentralrs1064796360
openSNPrs1064796360
23andMers1064796360
23andMe allrs1064796360
SNPshotrs1064796360
SNPdbers1064796360
MSV3drs1064796360
GWAS Ctlgrs1064796360
Max Magnitude0
ClinVar
Risk rs1064796360(-;-)
Alt rs1064796360(-;-)
Reference Rs1064796360(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CCDC39
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.180359911delC
CLNSRC
CLNACC RCV000483655.1,