Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057520565

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520565(C;T)
Make rs1057520565(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89279404
GeneANKRD11
is asnp
is mentioned by
dbSNPrs1057520565
dbSNP (old)rs1057520565
ClinGenrs1057520565
ebirs1057520565
HLIrs1057520565
Exacrs1057520565
Gnomadrs1057520565
Varsomers1057520565
LitVarrs1057520565
Maprs1057520565
PheGenIrs1057520565
Biobankrs1057520565
1000 genomesrs1057520565
hgdprs1057520565
ensemblrs1057520565
gopubmedrs1057520565
geneviewrs1057520565
scholarrs1057520565
googlers1057520565
pharmgkbrs1057520565
gwascentralrs1057520565
openSNPrs1057520565
23andMers1057520565
23andMe allrs1057520565
SNPshotrs1057520565
SNPdbers1057520565
MSV3drs1057520565
GWAS Ctlgrs1057520565
Max Magnitude0
ClinVar
Risk rs1057520565(T;T)
Alt rs1057520565(T;T)
Reference Rs1057520565(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ANKRD11
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.89345812G>A
CLNSRC
CLNACC RCV000425698.1,