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rs863225296

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225296(C;T)
Make rs863225296(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89279362
GeneANKRD11
is asnp
is mentioned by
dbSNPrs863225296
ebirs863225296
HLIrs863225296
Exacrs863225296
Varsomers863225296
Maprs863225296
PheGenIrs863225296
hapmaprs863225296
1000 genomesrs863225296
hgdprs863225296
ensemblrs863225296
gopubmedrs863225296
geneviewrs863225296
scholarrs863225296
googlers863225296
pharmgkbrs863225296
gwascentralrs863225296
openSNPrs863225296
23andMers863225296
23andMe allrs863225296
SNP Nexus

SNPshotrs863225296
SNPdbers863225296
MSV3drs863225296
GWAS Ctlgrs863225296
Max Magnitude0
ClinVar
Risk rs863225296(T;T)
Alt rs863225296(T;T)
Reference rs863225296(C;C)
Significance Pathogenic
Disease KBG syndrome
Variation info
Gene ANKRD11
CLNDBN KBG syndrome
Reversed 1
HGVS NC_000016.9:g.89345770G>A
CLNSRC
CLNACC RCV000201945.1,