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rs1064793988

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome20
Position32435522
GeneASXL1
is asnp
is mentioned by
dbSNPrs1064793988
dbSNP (old)rs1064793988
ClinGenrs1064793988
ebirs1064793988
HLIrs1064793988
Exacrs1064793988
Gnomadrs1064793988
Varsomers1064793988
LitVarrs1064793988
Maprs1064793988
PheGenIrs1064793988
Biobankrs1064793988
1000 genomesrs1064793988
hgdprs1064793988
ensemblrs1064793988
gopubmedrs1064793988
geneviewrs1064793988
scholarrs1064793988
googlers1064793988
pharmgkbrs1064793988
gwascentralrs1064793988
openSNPrs1064793988
23andMers1064793988
23andMe allrs1064793988
SNPshotrs1064793988
SNPdbers1064793988
MSV3drs1064793988
GWAS Ctlgrs1064793988
Max Magnitude0
ClinVar
Risk rs1064793988(-;-)
Alt rs1064793988(-;-)
Reference Rs1064793988(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ASXL1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.31023325delC
CLNSRC
CLNACC RCV000481700.1,