rs34022507

Orientation

minus

Stabilized

minus

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

Make rs34022507(C;T)

Make rs34022507(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

5225726

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs34022507
dbSNP (classic)	rs34022507
ClinGen	rs34022507
ebi	rs34022507
HLI	rs34022507
Exac	rs34022507
Gnomad	rs34022507
Varsome	rs34022507
LitVar	rs34022507
Map	rs34022507
PheGenI	rs34022507
Biobank	rs34022507
1000 genomes	rs34022507
hgdp	rs34022507
ensembl	rs34022507
geneview	rs34022507
scholar	rs34022507
google	rs34022507
pharmgkb	rs34022507
gwascentral	rs34022507
openSNP	rs34022507
23andMe	rs34022507
SNPshot	rs34022507
SNPdbe	rs34022507
MSV3d	rs34022507
GWAS Ctlg	rs34022507

Max Magnitude

0

OMIM	141900
Desc
Variant	0391
Related	also

ClinVar
Risk	rs34022507(T;T)
Alt	rs34022507(T;T)
Reference	Rs34022507(C;C)
Significance	Other
Disease	HEMOGLOBIN SOUTH MILWAUKEE
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN SOUTH MILWAUKEE
Reversed	1
HGVS	NC_000011.9:g.5246956G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016738.2,

[PMID 2363414] Hb south Milwaukee [beta 105 (G7) Leu----Phe]: a newly-identified hemoglobin variant with high oxygen affinity.