rs111033598

Orientation

plus

Stabilized

plus

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

Make rs111033598(C;C)

Make rs111033598(C;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

173212

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs111033598
dbSNP (classic)	rs111033598
ClinGen	rs111033598
ebi	rs111033598
HLI	rs111033598
Exac	rs111033598
Gnomad	rs111033598
Varsome	rs111033598
LitVar	rs111033598
Map	rs111033598
PheGenI	rs111033598
Biobank	rs111033598
1000 genomes	rs111033598
hgdp	rs111033598
ensembl	rs111033598
geneview	rs111033598
scholar	rs111033598
google	rs111033598
pharmgkb	rs111033598
gwascentral	rs111033598
openSNP	rs111033598
23andMe	rs111033598
SNPshot	rs111033598
SNPdbe	rs111033598
MSV3d	rs111033598
GWAS Ctlg	rs111033598

Max Magnitude

0

OMIM	141850
Desc
Variant	0008
Related	also

ClinVar
Risk	rs111033598(C;C) rs111033598(T;T)
Alt	rs111033598(C;C) rs111033598(T;T)
Reference	Rs111033598(G;G)
Significance	Untested
Disease
Variation	info
Gene	HBA2
CLNDBN
Reversed	0
HGVS	NC_000016.9:g.223211G>C; NC_000016.9:g.223211G>T
CLNSRC
CLNACC

[PMID 5356548] Abnormal haemoglobins in Zambia. A new haemoglobin Zambia alpha-60 (E9) lysine--asparagine.