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rs1057518987

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518987(-;-)
Make rs1057518987(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89280324
GeneANKRD11
is asnp
is mentioned by
dbSNPrs1057518987
dbSNP (old)rs1057518987
ClinGenrs1057518987
ebirs1057518987
HLIrs1057518987
Exacrs1057518987
Gnomadrs1057518987
Varsomers1057518987
Maprs1057518987
PheGenIrs1057518987
Biobankrs1057518987
1000 genomesrs1057518987
hgdprs1057518987
ensemblrs1057518987
gopubmedrs1057518987
geneviewrs1057518987
scholarrs1057518987
googlers1057518987
pharmgkbrs1057518987
gwascentralrs1057518987
openSNPrs1057518987
23andMers1057518987
23andMe allrs1057518987
SNPshotrs1057518987
SNPdbers1057518987
MSV3drs1057518987
GWAS Ctlgrs1057518987
Max Magnitude0
ClinVar
Risk rs1057518987(-;-)
Alt rs1057518987(-;-)
Reference Rs1057518987(C;C)
Significance Probable-Pathogenic
Disease Moderate intellectual deficiency
Variation info
Gene ANKRD11
CLNDBN Moderate intellectual deficiency
Reversed 1
HGVS NC_000016.9:g.89346732delG
CLNSRC
CLNACC RCV000415439.1,