rs63751471

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;CTCCCCGCCGAG)	3	Alpha-thalassemia allele carrier
(CTCCCCGCCGAG;CTCCCCGCCGAG)	0	common/normal

Make rs63751471(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

173511

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs63751471
dbSNP (classic)	rs63751471
ClinGen	rs63751471
ebi	rs63751471
HLI	rs63751471
Exac	rs63751471
Gnomad	rs63751471
Varsome	rs63751471
LitVar	rs63751471
Map	rs63751471
PheGenI	rs63751471
Biobank	rs63751471
1000 genomes	rs63751471
hgdp	rs63751471
ensembl	rs63751471
geneview	rs63751471
scholar	rs63751471
google	rs63751471
pharmgkb	rs63751471
gwascentral	rs63751471
openSNP	rs63751471
23andMe	rs63751471
SNPshot	rs63751471
SNPdbe	rs63751471
MSV3d	rs63751471
GWAS Ctlg	rs63751471

Max Magnitude

3

ClinVar
Risk	rs63751471(-;-)
Alt	rs63751471(-;-)
Reference	Rs63751471(CTCCCCGCCGAG;CTCCCCGCCGAG)
Significance	Pathogenic
Disease	Alpha Thalassemia
Variation	info
Gene	HBA2
CLNDBN	alpha Thalassemia
Reversed	0
HGVS	NC_000016.9:g.223510_223521delCTCCCCGCCGAG
CLNSRC
CLNACC	RCV000417222.1,