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rs751342087

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs751342087(-;G)
Make rs751342087(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position89145276
GeneACSF3
is asnp
is mentioned by
dbSNPrs751342087
dbSNP (classic)rs751342087
ClinGenrs751342087
ebirs751342087
HLIrs751342087
Exacrs751342087
Gnomadrs751342087
Varsomers751342087
LitVarrs751342087
Maprs751342087
PheGenIrs751342087
Biobankrs751342087
1000 genomesrs751342087
hgdprs751342087
ensemblrs751342087
geneviewrs751342087
scholarrs751342087
googlers751342087
pharmgkbrs751342087
gwascentralrs751342087
openSNPrs751342087
23andMers751342087
23andMe allrs751342087
SNPshotrs751342087
SNPdbers751342087
MSV3drs751342087
GWAS Ctlgrs751342087
Max Magnitude0
ClinVar
Risk rs751342087(G;G)
Alt rs751342087(G;G)
Reference Rs751342087(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACSF3
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.89211686dup
CLNSRC
CLNACC RCV000489924.2,