rs387907078

Orientation

plus

Stabilized

plus

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

Make rs387907078(C;T)

Make rs387907078(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

32434909

Gene

ASXL1

is a	snp
is	mentioned by
dbSNP	rs387907078
dbSNP (classic)	rs387907078
ClinGen	rs387907078
ebi	rs387907078
HLI	rs387907078
Exac	rs387907078
Gnomad	rs387907078
Varsome	rs387907078
LitVar	rs387907078
Map	rs387907078
PheGenI	rs387907078
Biobank	rs387907078
1000 genomes	rs387907078
hgdp	rs387907078
ensembl	rs387907078
geneview	rs387907078
scholar	rs387907078
google	rs387907078
pharmgkb	rs387907078
gwascentral	rs387907078
openSNP	rs387907078
23andMe	rs387907078
SNPshot	rs387907078
SNPdbe	rs387907078
MSV3d	rs387907078
GWAS Ctlg	rs387907078

Max Magnitude

0

ClinVar
Risk	rs387907078(T;T)
Alt	rs387907078(T;T)
Reference	Rs387907078(C;C)
Significance	Pathogenic
Disease	C-like syndrome
Variation	info
Gene	ASXL1
CLNDBN	C-like syndrome
Reversed	0
HGVS	NC_000020.10:g.31022712C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023980.2,