rs33937535

Orientation

minus

Stabilized

minus

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

Make rs33937535(A;C)

Make rs33937535(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5225650

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33937535
dbSNP (classic)	rs33937535
ClinGen	rs33937535
ebi	rs33937535
HLI	rs33937535
Exac	rs33937535
Gnomad	rs33937535
Varsome	rs33937535
LitVar	rs33937535
Map	rs33937535
PheGenI	rs33937535
Biobank	rs33937535
1000 genomes	rs33937535
hgdp	rs33937535
ensembl	rs33937535
geneview	rs33937535
scholar	rs33937535
google	rs33937535
pharmgkb	rs33937535
gwascentral	rs33937535
openSNP	rs33937535
23andMe	rs33937535
SNPshot	rs33937535
SNPdbe	rs33937535
MSV3d	rs33937535
GWAS Ctlg	rs33937535

Max Magnitude

0

OMIM	141900
Desc
Variant	0194
Related	also

ClinVar
Risk	rs33937535(C;C) rs33937535(G;G)
Alt	rs33937535(C;C) rs33937535(G;G)
Reference	Rs33937535(A;A)
Significance	Other
Disease	HEMOGLOBIN NEVERS
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN NEVERS
Reversed	1
HGVS	NC_000011.9:g.5246880T>G
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016514.2,

[PMID 2384309] Hemoglobin Nevers [alpha 2 beta 2130(H8)Tyr----Ser]; a new silent variant found in France.