Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057521852

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521852(A;C)
Make rs1057521852(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position47985531
GeneCOL2A1
is asnp
is mentioned by
dbSNPrs1057521852
dbSNP (old)rs1057521852
ClinGenrs1057521852
ebirs1057521852
HLIrs1057521852
Exacrs1057521852
Gnomadrs1057521852
Varsomers1057521852
Maprs1057521852
PheGenIrs1057521852
Biobankrs1057521852
1000 genomesrs1057521852
hgdprs1057521852
ensemblrs1057521852
gopubmedrs1057521852
geneviewrs1057521852
scholarrs1057521852
googlers1057521852
pharmgkbrs1057521852
gwascentralrs1057521852
openSNPrs1057521852
23andMers1057521852
23andMe allrs1057521852
SNPshotrs1057521852
SNPdbers1057521852
MSV3drs1057521852
GWAS Ctlgrs1057521852
Max Magnitude0
ClinVar
Risk rs1057521852(C;C)
Alt rs1057521852(C;C)
Reference Rs1057521852(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL2A1
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.48379314T>G
CLNSRC
CLNACC RCV000422960.1,