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rs1064796332

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome12
Position47987113
GeneCOL2A1
is asnp
is mentioned by
dbSNPrs1064796332
dbSNP (old)rs1064796332
ClinGenrs1064796332
ebirs1064796332
HLIrs1064796332
Exacrs1064796332
Gnomadrs1064796332
Varsomers1064796332
Maprs1064796332
PheGenIrs1064796332
Biobankrs1064796332
1000 genomesrs1064796332
hgdprs1064796332
ensemblrs1064796332
gopubmedrs1064796332
geneviewrs1064796332
scholarrs1064796332
googlers1064796332
pharmgkbrs1064796332
gwascentralrs1064796332
openSNPrs1064796332
23andMers1064796332
23andMe allrs1064796332
SNPshotrs1064796332
SNPdbers1064796332
MSV3drs1064796332
GWAS Ctlgrs1064796332
Max Magnitude0
ClinVar
Risk rs1064796332(A;A)
Alt rs1064796332(A;A)
Reference Rs1064796332(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL2A1
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.48380896C>T
CLNSRC
CLNACC RCV000483756.1,