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rs797044890

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044890(A;A)
Make rs797044890(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89275092
GeneANKRD11
is asnp
is mentioned by
dbSNPrs797044890
ebirs797044890
HLIrs797044890
Exacrs797044890
Varsomers797044890
Maprs797044890
PheGenIrs797044890
hapmaprs797044890
1000 genomesrs797044890
hgdprs797044890
ensemblrs797044890
gopubmedrs797044890
geneviewrs797044890
scholarrs797044890
googlers797044890
pharmgkbrs797044890
gwascentralrs797044890
openSNPrs797044890
23andMers797044890
23andMe allrs797044890
SNP Nexus

SNPshotrs797044890
SNPdbers797044890
MSV3drs797044890
GWAS Ctlgrs797044890
Max Magnitude0
ClinVar
Risk rs797044890(A;A)
Alt rs797044890(A;A)
Reference rs797044890(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene ANKRD11
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000016.9:g.89341500C>T
CLNSRC
CLNACC RCV000190712.1,