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rs886039743

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039743(A;A)
Make rs886039743(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position103006314
GeneCOL11A1
is asnp
is mentioned by
dbSNPrs886039743
dbSNP (classic)rs886039743
ClinGenrs886039743
ebirs886039743
HLIrs886039743
Exacrs886039743
Gnomadrs886039743
Varsomers886039743
LitVarrs886039743
Maprs886039743
PheGenIrs886039743
Biobankrs886039743
1000 genomesrs886039743
hgdprs886039743
ensemblrs886039743
geneviewrs886039743
scholarrs886039743
googlers886039743
pharmgkbrs886039743
gwascentralrs886039743
openSNPrs886039743
23andMers886039743
SNPshotrs886039743
SNPdbers886039743
MSV3drs886039743
GWAS Ctlgrs886039743
Max Magnitude0
ClinVar
Risk rs886039743(A;A)
Alt rs886039743(A;A)
Reference Rs886039743(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL11A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.103471870C>T
CLNSRC
CLNACC RCV000255656.1,