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rs886039722

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs886039722(A;A)
Make rs886039722(A;C)
ReferenceGRCh38.p7 38.3/149
Chromosome20
Position32435634
GeneASXL1
is asnp
is mentioned by
dbSNPrs886039722
dbSNP (classic)rs886039722
ClinGenrs886039722
ebirs886039722
HLIrs886039722
Exacrs886039722
Gnomadrs886039722
Varsomers886039722
LitVarrs886039722
Maprs886039722
PheGenIrs886039722
Biobankrs886039722
1000 genomesrs886039722
hgdprs886039722
ensemblrs886039722
geneviewrs886039722
scholarrs886039722
googlers886039722
pharmgkbrs886039722
gwascentralrs886039722
openSNPrs886039722
23andMers886039722
23andMe allrs886039722
SNPshotrs886039722
SNPdbers886039722
MSV3drs886039722
GWAS Ctlgrs886039722
Max Magnitude0
ClinVar
Risk rs886039722(A;A)
Alt rs886039722(A;A)
Reference Rs886039722(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ASXL1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.31023437C>A
CLNSRC
CLNACC RCV000255194.1,