rs786205552

Orientation

plus

Stabilized

plus

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

Make rs786205552(C;C)

Make rs786205552(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

20

Position

32435701

Gene

ASXL1

is a	snp
is	mentioned by
dbSNP	rs786205552
dbSNP (classic)	rs786205552
ClinGen	rs786205552
ebi	rs786205552
HLI	rs786205552
Exac	rs786205552
Gnomad	rs786205552
Varsome	rs786205552
LitVar	rs786205552
Map	rs786205552
PheGenI	rs786205552
Biobank	rs786205552
1000 genomes	rs786205552
hgdp	rs786205552
ensembl	rs786205552
geneview	rs786205552
scholar	rs786205552
google	rs786205552
pharmgkb	rs786205552
gwascentral	rs786205552
openSNP	rs786205552
23andMe	rs786205552
SNPshot	rs786205552
SNPdbe	rs786205552
MSV3d	rs786205552
GWAS Ctlg	rs786205552

Max Magnitude

0

ClinVar
Risk	rs786205552(C;C)
Alt	rs786205552(C;C)
Reference	Rs786205552(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ASXL1
CLNDBN	not provided
Reversed	0
HGVS	NC_000020.10:g.31023504G>C
CLNSRC
CLNACC	RCV000171345.1,