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rs772229371

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs772229371(G;T)
Make rs772229371(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position89284741
GeneANKRD11
is asnp
is mentioned by
dbSNPrs772229371
dbSNP (classic)rs772229371
ClinGenrs772229371
ebirs772229371
HLIrs772229371
Exacrs772229371
Gnomadrs772229371
Varsomers772229371
LitVarrs772229371
Maprs772229371
PheGenIrs772229371
Biobankrs772229371
1000 genomesrs772229371
hgdprs772229371
ensemblrs772229371
geneviewrs772229371
scholarrs772229371
googlers772229371
pharmgkbrs772229371
gwascentralrs772229371
openSNPrs772229371
23andMers772229371
SNPshotrs772229371
SNPdbers772229371
MSV3drs772229371
GWAS Ctlgrs772229371
Max Magnitude0
ClinVar
Risk rs772229371(A;A) rs772229371(T;T)
Alt rs772229371(A;A) rs772229371(T;T)
Reference Rs772229371(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ANKRD11
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89351149G>A
CLNSRC
CLNACC RCV000317010.1,