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rs1064794293

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome19
Position18785808
GeneCOMP
is asnp
is mentioned by
dbSNPrs1064794293
dbSNP (old)rs1064794293
ClinGenrs1064794293
ebirs1064794293
HLIrs1064794293
Exacrs1064794293
Gnomadrs1064794293
Varsomers1064794293
Maprs1064794293
PheGenIrs1064794293
Biobankrs1064794293
1000 genomesrs1064794293
hgdprs1064794293
ensemblrs1064794293
gopubmedrs1064794293
geneviewrs1064794293
scholarrs1064794293
googlers1064794293
pharmgkbrs1064794293
gwascentralrs1064794293
openSNPrs1064794293
23andMers1064794293
23andMe allrs1064794293
SNPshotrs1064794293
SNPdbers1064794293
MSV3drs1064794293
GWAS Ctlgrs1064794293
Max Magnitude0
ClinVar
Risk rs1064794293(G;G)
Alt rs1064794293(G;G)
Reference Rs1064794293(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COMP
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.18896618G>C
CLNSRC
CLNACC RCV000483120.1,