rs63749934

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs63749934(C;C)

Make rs63749934(C;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

173196

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs63749934
dbSNP (classic)	rs63749934
ClinGen	rs63749934
ebi	rs63749934
HLI	rs63749934
Exac	rs63749934
Gnomad	rs63749934
Varsome	rs63749934
LitVar	rs63749934
Map	rs63749934
PheGenI	rs63749934
Biobank	rs63749934
1000 genomes	rs63749934
hgdp	rs63749934
ensembl	rs63749934
geneview	rs63749934
scholar	rs63749934
google	rs63749934
pharmgkb	rs63749934
gwascentral	rs63749934
openSNP	rs63749934
23andMe	rs63749934
SNPshot	rs63749934
SNPdbe	rs63749934
MSV3d	rs63749934
GWAS Ctlg	rs63749934

Max Magnitude

0

OMIM	141850
Desc
Variant	0046
Related	also

ClinVar
Risk	rs63749934(C;C)
Alt	rs63749934(C;C)
Reference	Rs63749934(T;T)
Significance	Other
Disease	HEMOGLOBIN GERLAND
Variation	info
Gene	HBA2
CLNDBN	HEMOGLOBIN GERLAND
Reversed	0
HGVS	NC_000016.9:g.223195T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016956.1,

[PMID 11791875] Hb Gerland [alpha55(E4)Val-->Ala (alpha2)]: a new neutral alpha chain variant involving the alpha2 gene.