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rs1057524696

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524696(C;C)
Make rs1057524696(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position47985727
GeneCOL2A1
is asnp
is mentioned by
dbSNPrs1057524696
dbSNP (old)rs1057524696
ClinGenrs1057524696
ebirs1057524696
HLIrs1057524696
Exacrs1057524696
Gnomadrs1057524696
Varsomers1057524696
Maprs1057524696
PheGenIrs1057524696
Biobankrs1057524696
1000 genomesrs1057524696
hgdprs1057524696
ensemblrs1057524696
gopubmedrs1057524696
geneviewrs1057524696
scholarrs1057524696
googlers1057524696
pharmgkbrs1057524696
gwascentralrs1057524696
openSNPrs1057524696
23andMers1057524696
23andMe allrs1057524696
SNPshotrs1057524696
SNPdbers1057524696
MSV3drs1057524696
GWAS Ctlgrs1057524696
Max Magnitude0
ClinVar
Risk rs1057524696(C;C)
Alt rs1057524696(C;C)
Reference Rs1057524696(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL2A1
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.48379510C>G
CLNSRC
CLNACC RCV000426239.1,