rs41515649

Orientation

plus

Stabilized

plus

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

Make rs41515649(A;A)

Make rs41515649(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

173216

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs41515649
dbSNP (classic)	rs41515649
ClinGen	rs41515649
ebi	rs41515649
HLI	rs41515649
Exac	rs41515649
Gnomad	rs41515649
Varsome	rs41515649
LitVar	rs41515649
Map	rs41515649
PheGenI	rs41515649
Biobank	rs41515649
1000 genomes	rs41515649
hgdp	rs41515649
ensembl	rs41515649
geneview	rs41515649
scholar	rs41515649
google	rs41515649
pharmgkb	rs41515649
gwascentral	rs41515649
openSNP	rs41515649
23andMe	rs41515649
SNPshot	rs41515649
SNPdbe	rs41515649
MSV3d	rs41515649
GWAS Ctlg	rs41515649

Max Magnitude

0

OMIM	141850
Desc
Variant	0006
Related	also

ClinVar
Risk	rs41515649(A;A)
Alt	rs41515649(A;A)
Reference	Rs41515649(G;G)
Significance	Other
Disease	HEMOGLOBIN EVANS
Variation	info
Gene	HBA2
CLNDBN	HEMOGLOBIN EVANS
Reversed	0
HGVS	NC_000016.9:g.223215G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016898.1,

[PMID 2606724] Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia.