rs886039722

Orientation

plus

Stabilized

plus

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

Make rs886039722(A;A)

Make rs886039722(A;C)

Reference

GRCh38.p7 38.3/149

Chromosome

20

Position

32435634

Gene

ASXL1

is a	snp
is	mentioned by
dbSNP	rs886039722
dbSNP (classic)	rs886039722
ClinGen	rs886039722
ebi	rs886039722
HLI	rs886039722
Exac	rs886039722
Gnomad	rs886039722
Varsome	rs886039722
LitVar	rs886039722
Map	rs886039722
PheGenI	rs886039722
Biobank	rs886039722
1000 genomes	rs886039722
hgdp	rs886039722
ensembl	rs886039722
geneview	rs886039722
scholar	rs886039722
google	rs886039722
pharmgkb	rs886039722
gwascentral	rs886039722
openSNP	rs886039722
23andMe	rs886039722
SNPshot	rs886039722
SNPdbe	rs886039722
MSV3d	rs886039722
GWAS Ctlg	rs886039722

Max Magnitude

0

ClinVar
Risk	rs886039722(A;A)
Alt	rs886039722(A;A)
Reference	Rs886039722(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ASXL1
CLNDBN	not provided
Reversed	0
HGVS	NC_000020.10:g.31023437C>A
CLNSRC
CLNACC	RCV000255194.1,