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rs886041485

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Chromosome20
Position32433742
GeneASXL1
is asnp
is mentioned by
dbSNPrs886041485
dbSNP (classic)rs886041485
ClinGenrs886041485
ebirs886041485
HLIrs886041485
Exacrs886041485
Gnomadrs886041485
Varsomers886041485
LitVarrs886041485
Maprs886041485
PheGenIrs886041485
Biobankrs886041485
1000 genomesrs886041485
hgdprs886041485
ensemblrs886041485
geneviewrs886041485
scholarrs886041485
googlers886041485
pharmgkbrs886041485
gwascentralrs886041485
openSNPrs886041485
23andMers886041485
23andMe allrs886041485
SNPshotrs886041485
SNPdbers886041485
MSV3drs886041485
GWAS Ctlgrs886041485
Max Magnitude0
ClinVar
Risk rs886041485(-;-)
Alt rs886041485(-;-)
Reference Rs886041485(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene ASXL1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.31021545_31021546delTG
CLNSRC
CLNACC RCV000366685.1,