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rs886039734

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAAA;CAAA) 0 common in clinvar
Make rs886039734(-;-)
Make rs886039734(-;CAAA)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position89284364
GeneANKRD11
is asnp
is mentioned by
dbSNPrs886039734
dbSNP (classic)rs886039734
ClinGenrs886039734
ebirs886039734
HLIrs886039734
Exacrs886039734
Gnomadrs886039734
Varsomers886039734
LitVarrs886039734
Maprs886039734
PheGenIrs886039734
Biobankrs886039734
1000 genomesrs886039734
hgdprs886039734
ensemblrs886039734
geneviewrs886039734
scholarrs886039734
googlers886039734
pharmgkbrs886039734
gwascentralrs886039734
openSNPrs886039734
23andMers886039734
SNPshotrs886039734
SNPdbers886039734
MSV3drs886039734
GWAS Ctlgrs886039734
Max Magnitude0
ClinVar
Risk rs886039734(-;-)
Alt rs886039734(-;-)
Reference Rs886039734(CAAA;CAAA)
Significance Other
Disease not provided
Variation info
Gene ANKRD11
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.89350772_89350775delTTTG
CLNSRC
CLNACC RCV000255546.2,