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rs911722283

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position33171805
GeneCOL11A2
is asnp
is mentioned by
dbSNPrs911722283
dbSNP (classic)rs911722283
ClinGenrs911722283
ebirs911722283
HLIrs911722283
Exacrs911722283
Gnomadrs911722283
Varsomers911722283
LitVarrs911722283
Maprs911722283
PheGenIrs911722283
Biobankrs911722283
1000 genomesrs911722283
hgdprs911722283
ensemblrs911722283
geneviewrs911722283
scholarrs911722283
googlers911722283
pharmgkbrs911722283
gwascentralrs911722283
openSNPrs911722283
23andMers911722283
SNPshotrs911722283
SNPdbers911722283
MSV3drs911722283
GWAS Ctlgrs911722283
Max Magnitude0
ClinVar
Risk rs911722283(A;A)
Alt rs911722283(A;A)
Reference Rs911722283(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.33139582G>A
CLNSRC
CLNACC RCV000487207.1,