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

rs797044915

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044915(G;T)
Make rs797044915(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position33176015
GeneCOL11A2
is asnp
is mentioned by
dbSNPrs797044915
ebirs797044915
HLIrs797044915
Exacrs797044915
Varsomers797044915
Maprs797044915
PheGenIrs797044915
hapmaprs797044915
1000 genomesrs797044915
hgdprs797044915
ensemblrs797044915
gopubmedrs797044915
geneviewrs797044915
scholarrs797044915
googlers797044915
pharmgkbrs797044915
gwascentralrs797044915
openSNPrs797044915
23andMers797044915
23andMe allrs797044915
SNP Nexus

SNPshotrs797044915
SNPdbers797044915
MSV3drs797044915
GWAS Ctlgrs797044915
Max Magnitude0
ClinVar
Risk rs797044915(T;T)
Alt rs797044915(T;T)
Reference rs797044915(G;G)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene COL11A2
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000006.11:g.33143792C>A
CLNSRC
CLNACC RCV000190748.1,