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rs1064796772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Chromosome20
Position32435678
GeneASXL1
is asnp
is mentioned by
dbSNPrs1064796772
dbSNP (old)rs1064796772
ClinGenrs1064796772
ebirs1064796772
HLIrs1064796772
Exacrs1064796772
Gnomadrs1064796772
Varsomers1064796772
Maprs1064796772
PheGenIrs1064796772
Biobankrs1064796772
1000 genomesrs1064796772
hgdprs1064796772
ensemblrs1064796772
gopubmedrs1064796772
geneviewrs1064796772
scholarrs1064796772
googlers1064796772
pharmgkbrs1064796772
gwascentralrs1064796772
openSNPrs1064796772
23andMers1064796772
23andMe allrs1064796772
SNPshotrs1064796772
SNPdbers1064796772
MSV3drs1064796772
GWAS Ctlgrs1064796772
Max Magnitude0
ClinVar
Risk rs1064796772(-;-)
Alt rs1064796772(-;-)
Reference Rs1064796772(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene ASXL1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.31023481_31023482delCT
CLNSRC
CLNACC RCV000481961.1,