rs111316898

Orientation

plus

Stabilized

plus

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

Make rs111316898(C;T)

Make rs111316898(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

20

Position

32434579

Gene

ASXL1

is a	snp
is	mentioned by
dbSNP	rs111316898
dbSNP (classic)	rs111316898
ClinGen	rs111316898
ebi	rs111316898
HLI	rs111316898
Exac	rs111316898
Gnomad	rs111316898
Varsome	rs111316898
LitVar	rs111316898
Map	rs111316898
PheGenI	rs111316898
Biobank	rs111316898
1000 genomes	rs111316898
hgdp	rs111316898
ensembl	rs111316898
geneview	rs111316898
scholar	rs111316898
google	rs111316898
pharmgkb	rs111316898
gwascentral	rs111316898
openSNP	rs111316898
23andMe	rs111316898
SNPshot	rs111316898
SNPdbe	rs111316898
MSV3d	rs111316898
GWAS Ctlg	rs111316898

Max Magnitude

0

ClinVar
Risk	rs111316898(T;T)
Alt	rs111316898(T;T)
Reference	Rs111316898(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ASXL1
CLNDBN	not provided
Reversed	0
HGVS	NC_000020.10:g.31022382C>T
CLNSRC
CLNACC	RCV000331527.1,