rs33918778

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar
(GT;GT)	0	common in clinvar

Make rs33918778(G;T)

Make rs33918778(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226769

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33918778
dbSNP (classic)	rs33918778
ClinGen	rs33918778
ebi	rs33918778
HLI	rs33918778
Exac	rs33918778
Gnomad	rs33918778
Varsome	rs33918778
LitVar	rs33918778
Map	rs33918778
PheGenI	rs33918778
Biobank	rs33918778
1000 genomes	rs33918778
hgdp	rs33918778
ensembl	rs33918778
geneview	rs33918778
scholar	rs33918778
google	rs33918778
pharmgkb	rs33918778
gwascentral	rs33918778
openSNP	rs33918778
23andMe	rs33918778
SNPshot	rs33918778
SNPdbe	rs33918778
MSV3d	rs33918778
GWAS Ctlg	rs33918778

Max Magnitude

0

OMIM	141900
Desc
Variant	0014
Related	also

ClinVar
Risk	rs33918778(C;C) rs33918778(T;T)
Alt	rs33918778(C;C) rs33918778(T;T)
Reference	Rs33918778(G;G)
Significance	Other
Disease	HEMOGLOBIN AUSTIN
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN AUSTIN
Reversed	1
HGVS	NC_000011.9:g.5247999C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016256.3,

[PMID 14597] Hemoglobins Austin and Waco: two hemoglobins with substitutions in the alpha 1 beta 2 contact region.