rs33924825

Orientation

minus

Stabilized

minus

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

Make rs33924825(C;C)

Make rs33924825(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5249786

Gene

HBG1

is a	snp
is	mentioned by
dbSNP	rs33924825
dbSNP (classic)	rs33924825
ClinGen	rs33924825
ebi	rs33924825
HLI	rs33924825
Exac	rs33924825
Gnomad	rs33924825
Varsome	rs33924825
LitVar	rs33924825
Map	rs33924825
PheGenI	rs33924825
Biobank	rs33924825
1000 genomes	rs33924825
hgdp	rs33924825
ensembl	rs33924825
geneview	rs33924825
scholar	rs33924825
google	rs33924825
pharmgkb	rs33924825
gwascentral	rs33924825
openSNP	rs33924825
23andMe	rs33924825
SNPshot	rs33924825
SNPdbe	rs33924825
MSV3d	rs33924825
GWAS Ctlg	rs33924825

Max Magnitude

0

OMIM	142200
Desc
Variant	0017
Related	also

ClinVar
Risk	rs33924825(A;A) rs33924825(C;C)
Alt	rs33924825(A;A) rs33924825(C;C)
Reference	Rs33924825(G;G)
Significance	Other
Disease	HEMOGLOBIN F (PORDENONE)
Variation	info
Gene	HBG1
CLNDBN	HEMOGLOBIN F (PORDENONE)
Reversed	1
HGVS	NC_000011.9:g.5271016C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016161.1,

[PMID 6183236] A new gamma chain variant: Hb F-Pordenone [gamma 6(A3) Glu replaced by Gln: 75ILE: 136ALA].

[PMID 5635604] Haemoglobin F Texas II (alpha-2 gamma-2, 6 Glu-Lys), the second of the haemogloin F Texas variants.