rs193922563

Orientation

minus

Stabilized

minus

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

Make rs193922563(-;-)

Make rs193922563(-;TGGTCTATTTTCCCACCCTTAGGCT)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226797

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs193922563
dbSNP (classic)	rs193922563
ClinGen	rs193922563
ebi	rs193922563
HLI	rs193922563
Exac	rs193922563
Gnomad	rs193922563
Varsome	rs193922563
LitVar	rs193922563
Map	rs193922563
PheGenI	rs193922563
Biobank	rs193922563
1000 genomes	rs193922563
hgdp	rs193922563
ensembl	rs193922563
geneview	rs193922563
scholar	rs193922563
google	rs193922563
pharmgkb	rs193922563
gwascentral	rs193922563
openSNP	rs193922563
23andMe	rs193922563
SNPshot	rs193922563
SNPdbe	rs193922563
MSV3d	rs193922563
GWAS Ctlg	rs193922563

Max Magnitude

0

ClinVar
Risk	rs193922563(-;-)
Alt	rs193922563(-;-)
Reference	Rs193922563(TGGTCTATTTTCCCACCCTTAGGCT;TGGTCTATTTTCCCACCCTTAGGCT)
Significance	Pathogenic
Disease	beta^0^ Thalassemia Beta Thalassemia
Variation	info
Gene	HBB
CLNDBN	beta^0^ Thalassemia beta Thalassemia
Reversed	1
HGVS	NC_000011.9:g.5248027_5248051del25
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000016700.26, RCV000030009.1,