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rs761848111

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761848111(A;A)
Make rs761848111(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome16
Position89282980
GeneANKRD11
is asnp
is mentioned by
dbSNPrs761848111
dbSNP (classic)rs761848111
ClinGenrs761848111
ebirs761848111
HLIrs761848111
Exacrs761848111
Gnomadrs761848111
Varsomers761848111
LitVarrs761848111
Maprs761848111
PheGenIrs761848111
Biobankrs761848111
1000 genomesrs761848111
hgdprs761848111
ensemblrs761848111
geneviewrs761848111
scholarrs761848111
googlers761848111
pharmgkbrs761848111
gwascentralrs761848111
openSNPrs761848111
23andMers761848111
SNPshotrs761848111
SNPdbers761848111
MSV3drs761848111
GWAS Ctlgrs761848111
Max Magnitude0
ClinVar
Risk rs761848111(A;A)
Alt rs761848111(A;A)
Reference Rs761848111(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ANKRD11
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89349388G>A
CLNSRC
CLNACC RCV000266509.1,