rs33917394

Orientation

minus

Stabilized

minus

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

Make rs33917394(A;A)

Make rs33917394(A;C)

Reference

GRCh38 38.1/142

Chromosome

11

Position

5225699

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33917394
dbSNP (classic)	rs33917394
ClinGen	rs33917394
ebi	rs33917394
HLI	rs33917394
Exac	rs33917394
Gnomad	rs33917394
Varsome	rs33917394
LitVar	rs33917394
Map	rs33917394
PheGenI	rs33917394
Biobank	rs33917394
1000 genomes	rs33917394
hgdp	rs33917394
ensembl	rs33917394
geneview	rs33917394
scholar	rs33917394
google	rs33917394
pharmgkb	rs33917394
gwascentral	rs33917394
openSNP	rs33917394
23andMe	rs33917394
SNPshot	rs33917394
SNPdbe	rs33917394
MSV3d	rs33917394
GWAS Ctlg	rs33917394

Max Magnitude

0

OMIM	141900
Desc
Variant	0172
Related	also

OMIM	141900
Desc
Variant	0397
Related	also

ClinVar
Risk	rs33917394(A;A)
Alt	rs33917394(A;A)
Reference	Rs33917394(C;C)
Significance	Other
Disease	HEMOGLOBIN MASUDA HEMOGLOBIN ZENGCHENG
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN MASUDA HEMOGLOBIN ZENGCHENG
Reversed	1
HGVS	NC_000011.9:g.5246929G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016486.2, RCV000016745.3,

[PMID 2079435] Hb Zengcheng or alpha 2 beta(2)114(G16)Leu----Met.