rs397515401

Orientation

plus

Stabilized

plus

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

Make rs397515401(C;T)

Make rs397515401(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

32435605

Gene

ASXL1

is a	snp
is	mentioned by
dbSNP	rs397515401
dbSNP (classic)	rs397515401
ClinGen	rs397515401
ebi	rs397515401
HLI	rs397515401
Exac	rs397515401
Gnomad	rs397515401
Varsome	rs397515401
LitVar	rs397515401
Map	rs397515401
PheGenI	rs397515401
Biobank	rs397515401
1000 genomes	rs397515401
hgdp	rs397515401
ensembl	rs397515401
geneview	rs397515401
scholar	rs397515401
google	rs397515401
pharmgkb	rs397515401
gwascentral	rs397515401
openSNP	rs397515401
23andMe	rs397515401
SNPshot	rs397515401
SNPdbe	rs397515401
MSV3d	rs397515401
GWAS Ctlg	rs397515401

Max Magnitude

0

ClinVar
Risk	rs397515401(T;T)
Alt	rs397515401(T;T)
Reference	Rs397515401(C;C)
Significance	Pathogenic
Disease	C-like syndrome not provided
Variation	info
Gene	ASXL1
CLNDBN	C-like syndrome not provided
Reversed	0
HGVS	NC_000020.10:g.31023408C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000032665.2, RCV000255108.1,