Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057524831

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524831(C;T)
Make rs1057524831(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position33742891
GeneASXL3
is asnp
is mentioned by
dbSNPrs1057524831
dbSNP (old)rs1057524831
ClinGenrs1057524831
ebirs1057524831
HLIrs1057524831
Exacrs1057524831
Gnomadrs1057524831
Varsomers1057524831
Maprs1057524831
PheGenIrs1057524831
Biobankrs1057524831
1000 genomesrs1057524831
hgdprs1057524831
ensemblrs1057524831
gopubmedrs1057524831
geneviewrs1057524831
scholarrs1057524831
googlers1057524831
pharmgkbrs1057524831
gwascentralrs1057524831
openSNPrs1057524831
23andMers1057524831
23andMe allrs1057524831
SNPshotrs1057524831
SNPdbers1057524831
MSV3drs1057524831
GWAS Ctlgrs1057524831
Max Magnitude0
ClinVar
Risk rs1057524831(T;T)
Alt rs1057524831(T;T)
Reference Rs1057524831(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASXL3
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.31322855C>T
CLNSRC
CLNACC RCV000430452.1,