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rs1057519130

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519130(-;-)
Make rs1057519130(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position70300154
GeneCOL9A1
is asnp
is mentioned by
dbSNPrs1057519130
dbSNP (old)rs1057519130
ClinGenrs1057519130
ebirs1057519130
HLIrs1057519130
Exacrs1057519130
Gnomadrs1057519130
Varsomers1057519130
Maprs1057519130
PheGenIrs1057519130
Biobankrs1057519130
1000 genomesrs1057519130
hgdprs1057519130
ensemblrs1057519130
gopubmedrs1057519130
geneviewrs1057519130
scholarrs1057519130
googlers1057519130
pharmgkbrs1057519130
gwascentralrs1057519130
openSNPrs1057519130
23andMers1057519130
23andMe allrs1057519130
SNPshotrs1057519130
SNPdbers1057519130
MSV3drs1057519130
GWAS Ctlgrs1057519130
Max Magnitude0
ClinVar
Risk rs1057519130(-;-)
Alt rs1057519130(-;-)
Reference Rs1057519130(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL9A1
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.71009857delA
CLNSRC
CLNACC RCV000415882.1,