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rs768569721

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768569721(A;A)
Make rs768569721(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position33176294
GeneCOL11A2
is asnp
is mentioned by
dbSNPrs768569721
dbSNP (classic)rs768569721
ClinGenrs768569721
ebirs768569721
HLIrs768569721
Exacrs768569721
Gnomadrs768569721
Varsomers768569721
LitVarrs768569721
Maprs768569721
PheGenIrs768569721
Biobankrs768569721
1000 genomesrs768569721
hgdprs768569721
ensemblrs768569721
geneviewrs768569721
scholarrs768569721
googlers768569721
pharmgkbrs768569721
gwascentralrs768569721
openSNPrs768569721
23andMers768569721
SNPshotrs768569721
SNPdbers768569721
MSV3drs768569721
GWAS Ctlgrs768569721
Max Magnitude0
ClinVar
Risk rs768569721(A;A) rs768569721(T;T)
Alt rs768569721(A;A) rs768569721(T;T)
Reference Rs768569721(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL11A2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.33144071C>A
CLNSRC
CLNACC RCV000425711.1,