rs34769005

Orientation

minus

Stabilized

minus

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

Make rs34769005(C;G)

Make rs34769005(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5227005

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs34769005
dbSNP (classic)	rs34769005
ClinGen	rs34769005
ebi	rs34769005
HLI	rs34769005
Exac	rs34769005
Gnomad	rs34769005
Varsome	rs34769005
LitVar	rs34769005
Map	rs34769005
PheGenI	rs34769005
Biobank	rs34769005
1000 genomes	rs34769005
hgdp	rs34769005
ensembl	rs34769005
geneview	rs34769005
scholar	rs34769005
google	rs34769005
pharmgkb	rs34769005
gwascentral	rs34769005
openSNP	rs34769005
23andMe	rs34769005
SNPshot	rs34769005
SNPdbe	rs34769005
MSV3d	rs34769005
GWAS Ctlg	rs34769005

Max Magnitude

0

OMIM	141900
Desc
Variant	0296
Related	also

ClinVar
Risk	rs34769005(G;G) rs34769005(T;T)
Alt	rs34769005(G;G) rs34769005(T;T)
Reference	Rs34769005(C;C)
Significance	Other
Disease	HEMOGLOBIN WARWICKSHIRE
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN WARWICKSHIRE
Reversed	1
HGVS	NC_000011.9:g.5248235G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016640.2,

[PMID 6548451] Haemoglobin Warwickshire (beta 5 [A2] Pro----Arg). A possible 'fine tuning' of 2,3-DPG affinity by beta 5 Pro.