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rs796051924

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796051924(-;-)
Make rs796051924(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position89154194
GeneACSF3
is asnp
is mentioned by
dbSNPrs796051924
dbSNP (classic)rs796051924
ClinGenrs796051924
ebirs796051924
HLIrs796051924
Exacrs796051924
Gnomadrs796051924
Varsomers796051924
LitVarrs796051924
Maprs796051924
PheGenIrs796051924
Biobankrs796051924
1000 genomesrs796051924
hgdprs796051924
ensemblrs796051924
geneviewrs796051924
scholarrs796051924
googlers796051924
pharmgkbrs796051924
gwascentralrs796051924
openSNPrs796051924
23andMers796051924
SNPshotrs796051924
SNPdbers796051924
MSV3drs796051924
GWAS Ctlgrs796051924
Max Magnitude0
ClinVar
Risk rs796051924(-;-)
Alt rs796051924(-;-)
Reference Rs796051924(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACSF3
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89220602delT
CLNSRC
CLNACC RCV000185759.2,