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rs886039477

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs886039477(-;-)
Make rs886039477(-;AA)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position89282771
GeneANKRD11
is asnp
is mentioned by
dbSNPrs886039477
dbSNP (classic)rs886039477
ClinGenrs886039477
ebirs886039477
HLIrs886039477
Exacrs886039477
Gnomadrs886039477
Varsomers886039477
LitVarrs886039477
Maprs886039477
PheGenIrs886039477
Biobankrs886039477
1000 genomesrs886039477
hgdprs886039477
ensemblrs886039477
geneviewrs886039477
scholarrs886039477
googlers886039477
pharmgkbrs886039477
gwascentralrs886039477
openSNPrs886039477
23andMers886039477
23andMe allrs886039477
SNPshotrs886039477
SNPdbers886039477
MSV3drs886039477
GWAS Ctlgrs886039477
Max Magnitude0
ClinVar
Risk rs886039477(-;-)
Alt rs886039477(-;-)
Reference Rs886039477(AA;AA)
Significance Pathogenic
Disease not provided
Variation info
Gene ANKRD11
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.89349179_89349180delTT
CLNSRC
CLNACC RCV000256105.1,