rs398122842

Orientation

plus

Stabilized

plus

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

Make rs398122842(-;-)

Make rs398122842(-;GGGGGGG)

Reference

GRCh38.p2 38.2/144

Chromosome

19

Position

48955715

Gene

BAX

is a	snp
is	mentioned by
dbSNP	rs398122842
dbSNP (classic)	rs398122842
ClinGen	rs398122842
ebi	rs398122842
HLI	rs398122842
Exac	rs398122842
Gnomad	rs398122842
Varsome	rs398122842
LitVar	rs398122842
Map	rs398122842
PheGenI	rs398122842
Biobank	rs398122842
1000 genomes	rs398122842
hgdp	rs398122842
ensembl	rs398122842
geneview	rs398122842
scholar	rs398122842
google	rs398122842
pharmgkb	rs398122842
gwascentral	rs398122842
openSNP	rs398122842
23andMe	rs398122842
SNPshot	rs398122842
SNPdbe	rs398122842
MSV3d	rs398122842
GWAS Ctlg	rs398122842

Max Magnitude

0

ClinVar
Risk	rs398122842(-;-)
Alt	rs398122842(-;-)
Reference	Rs398122842(GGGGGGG;GGGGGGG)
Significance	Pathogenic
Disease	T-cell acute lymphoblastic leukemia
Variation	info
Gene	BAX
CLNDBN	T-cell acute lymphoblastic leukemia
Reversed	0
HGVS	NC_000019.9:g.49458972_49458978delGGGGGGG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010122.5,