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rs886039670

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs886039670(-;-)
Make rs886039670(-;TG)
Make rs886039670(TG;TG)
ReferenceGRCh38.p7 38.3/149
Chromosome20
Position32435856
GeneASXL1
is asnp
is mentioned by
dbSNPrs886039670
dbSNP (classic)rs886039670
ClinGenrs886039670
ebirs886039670
HLIrs886039670
Exacrs886039670
Gnomadrs886039670
Varsomers886039670
LitVarrs886039670
Maprs886039670
PheGenIrs886039670
Biobankrs886039670
1000 genomesrs886039670
hgdprs886039670
ensemblrs886039670
geneviewrs886039670
scholarrs886039670
googlers886039670
pharmgkbrs886039670
gwascentralrs886039670
openSNPrs886039670
23andMers886039670
23andMe allrs886039670
SNPshotrs886039670
SNPdbers886039670
MSV3drs886039670
GWAS Ctlgrs886039670
Max Magnitude0
ClinVar
Risk rs886039670(-;-)
Alt rs886039670(-;-)
Reference Rs886039670(GT;GT)
Significance Pathogenic
Disease not provided
Variation info
Gene ASXL1
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.31023659_31023660delTG
CLNSRC
CLNACC RCV000255751.1,