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rs886041791

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome16
Position89284345
GeneANKRD11
is asnp
is mentioned by
dbSNPrs886041791
dbSNP (classic)rs886041791
ClinGenrs886041791
ebirs886041791
HLIrs886041791
Exacrs886041791
Gnomadrs886041791
Varsomers886041791
LitVarrs886041791
Maprs886041791
PheGenIrs886041791
Biobankrs886041791
1000 genomesrs886041791
hgdprs886041791
ensemblrs886041791
geneviewrs886041791
scholarrs886041791
googlers886041791
pharmgkbrs886041791
gwascentralrs886041791
openSNPrs886041791
23andMers886041791
SNPshotrs886041791
SNPdbers886041791
MSV3drs886041791
GWAS Ctlgrs886041791
Max Magnitude0
ClinVar
Risk rs886041791(T;T)
Alt rs886041791(T;T)
Reference Rs886041791(C;C)
Significance Pathogenic
Disease not provided KBG syndrome
Variation info
Gene ANKRD11
CLNDBN not provided KBG syndrome
Reversed 1
HGVS NC_000016.9:g.89350753G>A
CLNSRC
CLNACC RCV000389598.1, RCV000455520.1,