rs35669628

Orientation

minus

Stabilized

minus

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

Make rs35669628(A;A)

Make rs35669628(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5225635

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs35669628
dbSNP (classic)	rs35669628
ClinGen	rs35669628
ebi	rs35669628
HLI	rs35669628
Exac	rs35669628
Gnomad	rs35669628
Varsome	rs35669628
LitVar	rs35669628
Map	rs35669628
PheGenI	rs35669628
Biobank	rs35669628
1000 genomes	rs35669628
hgdp	rs35669628
ensembl	rs35669628
geneview	rs35669628
scholar	rs35669628
google	rs35669628
pharmgkb	rs35669628
gwascentral	rs35669628
openSNP	rs35669628
23andMe	rs35669628
SNPshot	rs35669628
SNPdbe	rs35669628
MSV3d	rs35669628
GWAS Ctlg	rs35669628

Max Magnitude

0

OMIM	141900
Desc
Variant	0442
Related	also

ClinVar
Risk	rs35669628(A;A) rs35669628(T;T)
Alt	rs35669628(A;A) rs35669628(T;T)
Reference	Rs35669628(C;C)
Significance	Other
Disease	HEMOGLOBIN BECKMAN
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN BECKMAN
Reversed	1
HGVS	NC_000011.9:g.5246865G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016796.4,