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

rs1057517989

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517989(-;-)
Make rs1057517989(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position103008518
GeneCOL11A1
is asnp
is mentioned by
dbSNPrs1057517989
dbSNP (old)rs1057517989
ClinGenrs1057517989
ebirs1057517989
HLIrs1057517989
Exacrs1057517989
Gnomadrs1057517989
Varsomers1057517989
Maprs1057517989
PheGenIrs1057517989
Biobankrs1057517989
1000 genomesrs1057517989
hgdprs1057517989
ensemblrs1057517989
gopubmedrs1057517989
geneviewrs1057517989
scholarrs1057517989
googlers1057517989
pharmgkbrs1057517989
gwascentralrs1057517989
openSNPrs1057517989
23andMers1057517989
23andMe allrs1057517989
SNPshotrs1057517989
SNPdbers1057517989
MSV3drs1057517989
GWAS Ctlgrs1057517989
Max Magnitude0
ClinVar
Risk rs1057517989(-;-)
Alt rs1057517989(-;-)
Reference Rs1057517989(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene COL11A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.103474074delT
CLNSRC
CLNACC RCV000413570.1,