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

rs374156844

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs374156844(A;A)
Make rs374156844(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position33177700
GeneCOL11A2
is asnp
is mentioned by
dbSNPrs374156844
dbSNP (classic)rs374156844
ClinGenrs374156844
ebirs374156844
HLIrs374156844
Exacrs374156844
Gnomadrs374156844
Varsomers374156844
LitVarrs374156844
Maprs374156844
PheGenIrs374156844
Biobankrs374156844
1000 genomesrs374156844
hgdprs374156844
ensemblrs374156844
geneviewrs374156844
scholarrs374156844
googlers374156844
pharmgkbrs374156844
gwascentralrs374156844
openSNPrs374156844
23andMers374156844
SNPshotrs374156844
SNPdbers374156844
MSV3drs374156844
GWAS Ctlgrs374156844
Max Magnitude0
ClinVar
Risk rs374156844(A;A)
Alt rs374156844(A;A)
Reference Rs374156844(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL11A2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.33145477G>A
CLNSRC
CLNACC RCV000487615.1,