rs34264694

Orientation

minus

Stabilized

minus

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

Make rs34264694(A;C)

Make rs34264694(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5254408

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs34264694
dbSNP (classic)	rs34264694
ClinGen	rs34264694
ebi	rs34264694
HLI	rs34264694
Exac	rs34264694
Gnomad	rs34264694
Varsome	rs34264694
LitVar	rs34264694
Map	rs34264694
PheGenI	rs34264694
Biobank	rs34264694
1000 genomes	rs34264694
hgdp	rs34264694
ensembl	rs34264694
geneview	rs34264694
scholar	rs34264694
google	rs34264694
pharmgkb	rs34264694
gwascentral	rs34264694
openSNP	rs34264694
23andMe	rs34264694
SNPshot	rs34264694
SNPdbe	rs34264694
MSV3d	rs34264694
GWAS Ctlg	rs34264694

Max Magnitude

0

OMIM	142250
Desc
Variant	0031
Related	also

ClinVar
Risk	rs34264694(C;C)
Alt	rs34264694(C;C)
Reference	Rs34264694(A;A)
Significance	Other
Disease	HEMOGLOBIN F (BROOKLYN)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (BROOKLYN)
Reversed	1
HGVS	NC_000011.9:g.5275638T>G
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016127.1,

[PMID 1703138] Hb F-Brooklyn or alpha 2G gamma 2(66)(E10)Lys----Gln.