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rs886039241

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039241(A;A)
Make rs886039241(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome11
Position35663574
GeneTRIM44
is asnp
is mentioned by
dbSNPrs886039241
dbSNP (classic)rs886039241
ClinGenrs886039241
ebirs886039241
HLIrs886039241
Exacrs886039241
Gnomadrs886039241
Varsomers886039241
LitVarrs886039241
Maprs886039241
PheGenIrs886039241
Biobankrs886039241
1000 genomesrs886039241
hgdprs886039241
ensemblrs886039241
geneviewrs886039241
scholarrs886039241
googlers886039241
pharmgkbrs886039241
gwascentralrs886039241
openSNPrs886039241
23andMers886039241
SNPshotrs886039241
SNPdbers886039241
MSV3drs886039241
GWAS Ctlgrs886039241
Max Magnitude0
ClinVar
Risk rs886039241(A;A)
Alt rs886039241(A;A)
Reference Rs886039241(G;G)
Significance Pathogenic
Disease Aniridia 3
Variation info
Gene TRIM44
CLNDBN Aniridia 3
Reversed 0
HGVS NC_000011.9:g.35685122G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000254593.1,