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rs1064796916

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position209941467
GeneUNC80
is asnp
is mentioned by
dbSNPrs1064796916
dbSNP (classic)rs1064796916
ClinGenrs1064796916
ebirs1064796916
HLIrs1064796916
Exacrs1064796916
Gnomadrs1064796916
Varsomers1064796916
LitVarrs1064796916
Maprs1064796916
PheGenIrs1064796916
Biobankrs1064796916
1000 genomesrs1064796916
hgdprs1064796916
ensemblrs1064796916
geneviewrs1064796916
scholarrs1064796916
googlers1064796916
pharmgkbrs1064796916
gwascentralrs1064796916
openSNPrs1064796916
23andMers1064796916
23andMe allrs1064796916
SNPshotrs1064796916
SNPdbers1064796916
MSV3drs1064796916
GWAS Ctlgrs1064796916
Max Magnitude0
ClinVar
Risk rs1064796916(A;A)
Alt rs1064796916(A;A)
Reference Rs1064796916(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene UNC80
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.210806191G>A
CLNSRC
CLNACC RCV000486717.1,