rs34404985

Orientation

minus

Stabilized

minus

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

Make rs34404985(C;C)

Make rs34404985(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226946

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs34404985
dbSNP (classic)	rs34404985
ClinGen	rs34404985
ebi	rs34404985
HLI	rs34404985
Exac	rs34404985
Gnomad	rs34404985
Varsome	rs34404985
LitVar	rs34404985
Map	rs34404985
PheGenI	rs34404985
Biobank	rs34404985
1000 genomes	rs34404985
hgdp	rs34404985
ensembl	rs34404985
geneview	rs34404985
scholar	rs34404985
google	rs34404985
pharmgkb	rs34404985
gwascentral	rs34404985
openSNP	rs34404985
23andMe	rs34404985
SNPshot	rs34404985
SNPdbe	rs34404985
MSV3d	rs34404985
GWAS Ctlg	rs34404985

Max Magnitude

0

OMIM	141900
Desc
Variant	0089
Related	also

ClinVar
Risk	rs34404985(A;A) rs34404985(C;C)
Alt	rs34404985(A;A) rs34404985(C;C)
Reference	Rs34404985(G;G)
Significance	Other
Disease	HEMOGLOBIN G (TAIWAN-AMI)
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN G (TAIWAN-AMI)
Reversed	1
HGVS	NC_000011.9:g.5248176C>G
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016357.4,

[PMID 5642385] Hemoglobin G Taiwan-Ami: alpha-2-beta-225 Gly--Arg.