rs33935527

Orientation

minus

Stabilized

minus

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

Make rs33935527(C;T)

Make rs33935527(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5225690

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs33935527
dbSNP (classic)	rs33935527
ClinGen	rs33935527
ebi	rs33935527
HLI	rs33935527
Exac	rs33935527
Gnomad	rs33935527
Varsome	rs33935527
LitVar	rs33935527
Map	rs33935527
PheGenI	rs33935527
Biobank	rs33935527
1000 genomes	rs33935527
hgdp	rs33935527
ensembl	rs33935527
geneview	rs33935527
scholar	rs33935527
google	rs33935527
pharmgkb	rs33935527
gwascentral	rs33935527
openSNP	rs33935527
23andMe	rs33935527
SNPshot	rs33935527
SNPdbe	rs33935527
MSV3d	rs33935527
GWAS Ctlg	rs33935527

Max Magnitude

0

OMIM	141900
Desc
Variant	0494
Related	also

ClinVar
Risk	rs33935527(A;A) rs33935527(G;G) rs33935527(T;T)
Alt	rs33935527(A;A) rs33935527(G;G) rs33935527(T;T)
Reference	Rs33935527(C;C)
Significance	Untested
Disease
Variation	info
Gene	HBB
CLNDBN
Reversed	1
HGVS	NC_000011.9:g.5246920G>A; NC_000011.9:g.5246920G>C; NC_000011.9:g.5246920G>T
CLNSRC
CLNACC

[PMID 10870882] Hb Tsukumi [beta117(G19)His-->Tyr]: a new hemoglobin variant found in a Japanese male.

[PMID 11300344] Hb Tsukumi [beta117(G19)His-->Tyr] found in a Moroccan woman.

[PMID 10081991] Hb Brent [beta117(G19)His-->Asn]: a new hemoglobin variant found during routine antenatal screening.

[PMID 19205973] Hb North York [beta 117(G19)His-->Asp]: a new beta chain hemoglobin variant.