rs34173382

Orientation

minus

Stabilized

minus

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

Make rs34173382(A;G)

Make rs34173382(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226653

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs34173382
dbSNP (classic)	rs34173382
ClinGen	rs34173382
ebi	rs34173382
HLI	rs34173382
Exac	rs34173382
Gnomad	rs34173382
Varsome	rs34173382
LitVar	rs34173382
Map	rs34173382
PheGenI	rs34173382
Biobank	rs34173382
1000 genomes	rs34173382
hgdp	rs34173382
ensembl	rs34173382
geneview	rs34173382
scholar	rs34173382
google	rs34173382
pharmgkb	rs34173382
gwascentral	rs34173382
openSNP	rs34173382
23andMe	rs34173382
SNPshot	rs34173382
SNPdbe	rs34173382
MSV3d	rs34173382
GWAS Ctlg	rs34173382

Max Magnitude

0

OMIM	141900
Desc
Variant	0084
Related	also

ClinVar
Risk	rs34173382(G;G)
Alt	rs34173382(G;G)
Reference	Rs34173382(A;A)
Significance	Other
Disease	HEMOGLOBIN G (HSI-TSOU)
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN G (HSI-TSOU)
Reversed	1
HGVS	NC_000011.9:g.5247883T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016351.2,

[PMID 5009835] Hemoglobin G Hsi-Tsou: 79 Asp to Gly.