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rs1057518157

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518157(-;T)
Make rs1057518157(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position47977608
GeneCOL2A1
is asnp
is mentioned by
dbSNPrs1057518157
dbSNP (classic)rs1057518157
ClinGenrs1057518157
ebirs1057518157
HLIrs1057518157
Exacrs1057518157
Gnomadrs1057518157
Varsomers1057518157
LitVarrs1057518157
Maprs1057518157
PheGenIrs1057518157
Biobankrs1057518157
1000 genomesrs1057518157
hgdprs1057518157
ensemblrs1057518157
geneviewrs1057518157
scholarrs1057518157
googlers1057518157
pharmgkbrs1057518157
gwascentralrs1057518157
openSNPrs1057518157
23andMers1057518157
SNPshotrs1057518157
SNPdbers1057518157
MSV3drs1057518157
GWAS Ctlgrs1057518157
Max Magnitude0
ClinVar
Risk rs1057518157(T;T)
Alt rs1057518157(T;T)
Reference Rs1057518157(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene COL2A1
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.48371392dupA
CLNSRC
CLNACC RCV000414107.1,