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rs542568224

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs542568224(C;T)
Make rs542568224(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome20
Position32436347
GeneASXL1
is asnp
is mentioned by
dbSNPrs542568224
ebirs542568224
HLIrs542568224
Exacrs542568224
Varsomers542568224
Maprs542568224
PheGenIrs542568224
hapmaprs542568224
1000 genomesrs542568224
hgdprs542568224
ensemblrs542568224
gopubmedrs542568224
geneviewrs542568224
scholarrs542568224
googlers542568224
pharmgkbrs542568224
gwascentralrs542568224
openSNPrs542568224
23andMers542568224
23andMe allrs542568224
SNP Nexus

SNPshotrs542568224
SNPdbers542568224
MSV3drs542568224
GWAS Ctlgrs542568224
Max Magnitude0
ClinVar
Risk rs542568224(T;T)
Alt rs542568224(T;T)
Reference rs542568224(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASXL1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.31024150C>T
CLNSRC
CLNACC RCV000171346.1,