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rs886044913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome9
Position116699108
GeneASTN2, TRIM32
is asnp
is mentioned by
dbSNPrs886044913
dbSNP (classic)rs886044913
ClinGenrs886044913
ebirs886044913
HLIrs886044913
Exacrs886044913
Gnomadrs886044913
Varsomers886044913
LitVarrs886044913
Maprs886044913
PheGenIrs886044913
Biobankrs886044913
1000 genomesrs886044913
hgdprs886044913
ensemblrs886044913
geneviewrs886044913
scholarrs886044913
googlers886044913
pharmgkbrs886044913
gwascentralrs886044913
openSNPrs886044913
23andMers886044913
23andMe allrs886044913
SNPshotrs886044913
SNPdbers886044913
MSV3drs886044913
GWAS Ctlgrs886044913
Max Magnitude0
ClinVar
Risk rs886044913(TA;TA)
Alt rs886044913(TA;TA)
Reference Rs886044913(-;-)
Significance Pathogenic
Disease Elevated serum creatine phosphokinase
Variation info
Gene TRIM32 ASTN2
CLNDBN Elevated serum creatine phosphokinase
Reversed 0
HGVS NC_000009.11:g.119461386_119461387dupTA
CLNSRC
CLNACC RCV000306682.1,