rs41474145

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TGAGG)	3	Alpha-thalassemia allele carrier
(GAGGT;GAGGT)	0	common in clinvar
(TGAGG;TGAGG)	0	common/normal

Make rs41474145(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

173009

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs41474145
dbSNP (classic)	rs41474145
ClinGen	rs41474145
ebi	rs41474145
HLI	rs41474145
Exac	rs41474145
Gnomad	rs41474145
Varsome	rs41474145
LitVar	rs41474145
Map	rs41474145
PheGenI	rs41474145
Biobank	rs41474145
1000 genomes	rs41474145
hgdp	rs41474145
ensembl	rs41474145
geneview	rs41474145
scholar	rs41474145
google	rs41474145
pharmgkb	rs41474145
gwascentral	rs41474145
openSNP	rs41474145
23andMe	rs41474145
SNPshot	rs41474145
SNPdbe	rs41474145
MSV3d	rs41474145
GWAS Ctlg	rs41474145

Max Magnitude

3

ClinVar
Risk	rs41474145(-;-)
Alt	rs41474145(-;-)
Reference	Rs41474145(GAGGT;GAGGT)
Significance	Pathogenic
Disease	Alpha Thalassemia
Variation	info
Gene	HBA2
CLNDBN	alpha Thalassemia
Reversed	0
HGVS	NC_000016.9:g.223008_223012delTGAGG
CLNSRC
CLNACC	RCV000417225.1,