Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205477

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205477(G;T)
Make rs786205477(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position47977363
GeneCOL2A1
is asnp
is mentioned by
dbSNPrs786205477
ebirs786205477
HLIrs786205477
Exacrs786205477
Varsomers786205477
Maprs786205477
PheGenIrs786205477
hapmaprs786205477
1000 genomesrs786205477
hgdprs786205477
ensemblrs786205477
gopubmedrs786205477
geneviewrs786205477
scholarrs786205477
googlers786205477
pharmgkbrs786205477
gwascentralrs786205477
openSNPrs786205477
23andMers786205477
23andMe allrs786205477
SNP Nexus

SNPshotrs786205477
SNPdbers786205477
MSV3drs786205477
GWAS Ctlgrs786205477
Max Magnitude0
ClinVar
Risk rs786205477(T;T)
Alt rs786205477(T;T)
Reference rs786205477(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL2A1
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.48371146C>A
CLNSRC
CLNACC RCV000171212.1,