rs886039670

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GT;GT)	0	common in clinvar

Make rs886039670(-;-)

Make rs886039670(-;TG)

Make rs886039670(TG;TG)

Reference

GRCh38.p7 38.3/149

Chromosome

20

Position

32435856

Gene

ASXL1

is a	snp
is	mentioned by
dbSNP	rs886039670
dbSNP (classic)	rs886039670
ClinGen	rs886039670
ebi	rs886039670
HLI	rs886039670
Exac	rs886039670
Gnomad	rs886039670
Varsome	rs886039670
LitVar	rs886039670
Map	rs886039670
PheGenI	rs886039670
Biobank	rs886039670
1000 genomes	rs886039670
hgdp	rs886039670
ensembl	rs886039670
geneview	rs886039670
scholar	rs886039670
google	rs886039670
pharmgkb	rs886039670
gwascentral	rs886039670
openSNP	rs886039670
23andMe	rs886039670
SNPshot	rs886039670
SNPdbe	rs886039670
MSV3d	rs886039670
GWAS Ctlg	rs886039670

Max Magnitude

0

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,