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rs199800166

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199800166(C;T)
Make rs199800166(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89283858
GeneANKRD11
is asnp
is mentioned by
dbSNPrs199800166
dbSNP (old)rs199800166
ClinGenrs199800166
ebirs199800166
HLIrs199800166
Exacrs199800166
Gnomadrs199800166
Varsomers199800166
LitVarrs199800166
Maprs199800166
PheGenIrs199800166
Biobankrs199800166
1000 genomesrs199800166
hgdprs199800166
ensemblrs199800166
gopubmedrs199800166
geneviewrs199800166
scholarrs199800166
googlers199800166
pharmgkbrs199800166
gwascentralrs199800166
openSNPrs199800166
23andMers199800166
23andMe allrs199800166
SNPshotrs199800166
SNPdbers199800166
MSV3drs199800166
GWAS Ctlgrs199800166
Max Magnitude0
ClinVar
Risk rs199800166(T;T)
Alt rs199800166(T;T)
Reference Rs199800166(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ANKRD11
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89350266C>T
CLNSRC
CLNACC RCV000493061.1,