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rs797044900

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044900(C;T)
Make rs797044900(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89268645
GeneANKRD11
is asnp
is mentioned by
dbSNPrs797044900
ebirs797044900
HLIrs797044900
Exacrs797044900
Varsomers797044900
Maprs797044900
PheGenIrs797044900
hapmaprs797044900
1000 genomesrs797044900
hgdprs797044900
ensemblrs797044900
gopubmedrs797044900
geneviewrs797044900
scholarrs797044900
googlers797044900
pharmgkbrs797044900
gwascentralrs797044900
openSNPrs797044900
23andMers797044900
23andMe allrs797044900
SNP Nexus

SNPshotrs797044900
SNPdbers797044900
MSV3drs797044900
GWAS Ctlgrs797044900
Max Magnitude0
ClinVar
Risk rs797044900(T;T)
Alt rs797044900(T;T)
Reference rs797044900(C;C)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ANKRD11 LOC101927838
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000016.9:g.89335053G>A
CLNSRC
CLNACC RCV000190724.1,