Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057518578

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs1057518578(-;-)
Make rs1057518578(-;AA)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89281511
GeneANKRD11
is asnp
is mentioned by
dbSNPrs1057518578
dbSNP (old)rs1057518578
ClinGenrs1057518578
ebirs1057518578
HLIrs1057518578
Exacrs1057518578
Gnomadrs1057518578
Varsomers1057518578
Maprs1057518578
PheGenIrs1057518578
Biobankrs1057518578
1000 genomesrs1057518578
hgdprs1057518578
ensemblrs1057518578
gopubmedrs1057518578
geneviewrs1057518578
scholarrs1057518578
googlers1057518578
pharmgkbrs1057518578
gwascentralrs1057518578
openSNPrs1057518578
23andMers1057518578
23andMe allrs1057518578
SNPshotrs1057518578
SNPdbers1057518578
MSV3drs1057518578
GWAS Ctlgrs1057518578
Max Magnitude0
ClinVar
Risk rs1057518578(-;-)
Alt rs1057518578(-;-)
Reference Rs1057518578(AA;AA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ANKRD11
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.89347919_89347920delTT
CLNSRC
CLNACC RCV000413140.1,