rs41430445

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;T)	3	Alpha-thalassemia allele carrier
(T;T)	0	common in complete genomics

Make rs41430445(C;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

173130

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs41430445
dbSNP (classic)	rs41430445
ClinGen	rs41430445
ebi	rs41430445
HLI	rs41430445
Exac	rs41430445
Gnomad	rs41430445
Varsome	rs41430445
LitVar	rs41430445
Map	rs41430445
PheGenI	rs41430445
Biobank	rs41430445
1000 genomes	rs41430445
hgdp	rs41430445
ensembl	rs41430445
geneview	rs41430445
scholar	rs41430445
google	rs41430445
pharmgkb	rs41430445
gwascentral	rs41430445
openSNP	rs41430445
23andMe	rs41430445
SNPshot	rs41430445
SNPdbe	rs41430445
MSV3d	rs41430445
GWAS Ctlg	rs41430445

Max Magnitude

3

OMIM	141850
Desc
Variant	0058
Related	also

ClinVar
Risk	rs41430445(C;C)
Alt	rs41430445(C;C)
Reference	Rs41430445(T;T)
Significance	Other
Disease	HEMOGLOBIN CHARTRES
Variation	info
Gene	HBA2
CLNDBN	HEMOGLOBIN CHARTRES
Reversed	0
HGVS	NC_000016.9:g.223129T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016970.2,

[PMID 12779273] A new unstable alpha2-globin gene variant: Hb Chartres [alpha33(B14)Phe --> Ser].