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rs1064796170

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TCA;TCA) 0 common in clinvar
Chromosome12
Position47974238
GeneCOL2A1
is asnp
is mentioned by
dbSNPrs1064796170
dbSNP (classic)rs1064796170
ClinGenrs1064796170
ebirs1064796170
HLIrs1064796170
Exacrs1064796170
Gnomadrs1064796170
Varsomers1064796170
LitVarrs1064796170
Maprs1064796170
PheGenIrs1064796170
Biobankrs1064796170
1000 genomesrs1064796170
hgdprs1064796170
ensemblrs1064796170
geneviewrs1064796170
scholarrs1064796170
googlers1064796170
pharmgkbrs1064796170
gwascentralrs1064796170
openSNPrs1064796170
23andMers1064796170
SNPshotrs1064796170
SNPdbers1064796170
MSV3drs1064796170
GWAS Ctlgrs1064796170
Max Magnitude0
ClinVar
Risk rs1064796170(-;-)
Alt rs1064796170(-;-)
Reference Rs1064796170(TCA;TCA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL2A1
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.48368021_48368023delTGA
CLNSRC
CLNACC RCV000478499.1,