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rs886039902

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAAAA;AAAAA) 0 common in clinvar
Make rs886039902(-;-)
Make rs886039902(-;AAAAA)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position89284130
GeneANKRD11
is asnp
is mentioned by
dbSNPrs886039902
dbSNP (classic)rs886039902
ClinGenrs886039902
ebirs886039902
HLIrs886039902
Exacrs886039902
Gnomadrs886039902
Varsomers886039902
LitVarrs886039902
Maprs886039902
PheGenIrs886039902
Biobankrs886039902
1000 genomesrs886039902
hgdprs886039902
ensemblrs886039902
geneviewrs886039902
scholarrs886039902
googlers886039902
pharmgkbrs886039902
gwascentralrs886039902
openSNPrs886039902
23andMers886039902
SNPshotrs886039902
SNPdbers886039902
MSV3drs886039902
GWAS Ctlgrs886039902
Max Magnitude0
ClinVar
Risk rs886039902(-;-)
Alt rs886039902(-;-)
Reference Rs886039902(AAAAA;AAAAA)
Significance Pathogenic
Disease KBG syndrome
Variation info
Gene ANKRD11
CLNDBN KBG syndrome
Reversed 1
HGVS NC_000016.9:g.89350538_89350542delTTTTT
CLNSRC
CLNACC RCV000256444.1,