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rs766029215

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs766029215(A;A)
Make rs766029215(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position62821531
GeneCOL9A3
is asnp
is mentioned by
dbSNPrs766029215
dbSNP (classic)rs766029215
ClinGenrs766029215
ebirs766029215
HLIrs766029215
Exacrs766029215
Gnomadrs766029215
Varsomers766029215
LitVarrs766029215
Maprs766029215
PheGenIrs766029215
Biobankrs766029215
1000 genomesrs766029215
hgdprs766029215
ensemblrs766029215
geneviewrs766029215
scholarrs766029215
googlers766029215
pharmgkbrs766029215
gwascentralrs766029215
openSNPrs766029215
23andMers766029215
SNPshotrs766029215
SNPdbers766029215
MSV3drs766029215
GWAS Ctlgrs766029215
Max Magnitude0
ClinVar
Risk rs766029215(A;A)
Alt rs766029215(A;A)
Reference Rs766029215(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL9A3
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.61452883G>A
CLNSRC
CLNACC RCV000413769.1,