rs387907077

Orientation

plus

Stabilized

plus

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

Make rs387907077(C;T)

Make rs387907077(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

32435485

Gene

ASXL1

is a	snp
is	mentioned by
dbSNP	rs387907077
dbSNP (classic)	rs387907077
ClinGen	rs387907077
ebi	rs387907077
HLI	rs387907077
Exac	rs387907077
Gnomad	rs387907077
Varsome	rs387907077
LitVar	rs387907077
Map	rs387907077
PheGenI	rs387907077
Biobank	rs387907077
1000 genomes	rs387907077
hgdp	rs387907077
ensembl	rs387907077
geneview	rs387907077
scholar	rs387907077
google	rs387907077
pharmgkb	rs387907077
gwascentral	rs387907077
openSNP	rs387907077
23andMe	rs387907077
SNPshot	rs387907077
SNPdbe	rs387907077
MSV3d	rs387907077
GWAS Ctlg	rs387907077

Max Magnitude

0

ClinVar
Risk	rs387907077(T;T)
Alt	rs387907077(T;T)
Reference	Rs387907077(C;C)
Significance	Pathogenic
Disease	C-like syndrome
Variation	info
Gene	ASXL1
CLNDBN	C-like syndrome
Reversed	0
HGVS	NC_000020.10:g.31023288C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023976.2,