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rs886039713

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039713(A;A)
Make rs886039713(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position89284890
GeneANKRD11
is asnp
is mentioned by
dbSNPrs886039713
dbSNP (classic)rs886039713
ClinGenrs886039713
ebirs886039713
HLIrs886039713
Exacrs886039713
Gnomadrs886039713
Varsomers886039713
LitVarrs886039713
Maprs886039713
PheGenIrs886039713
Biobankrs886039713
1000 genomesrs886039713
hgdprs886039713
ensemblrs886039713
geneviewrs886039713
scholarrs886039713
googlers886039713
pharmgkbrs886039713
gwascentralrs886039713
openSNPrs886039713
23andMers886039713
SNPshotrs886039713
SNPdbers886039713
MSV3drs886039713
GWAS Ctlgrs886039713
Max Magnitude0
ClinVar
Risk rs886039713(A;A)
Alt rs886039713(A;A)
Reference Rs886039713(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ANKRD11
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.89351298C>T
CLNSRC
CLNACC RCV000255814.1,