rs35461710

Orientation

minus

Stabilized

minus

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

Make rs35461710(C;T)

Make rs35461710(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5225669

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs35461710
dbSNP (classic)	rs35461710
ClinGen	rs35461710
ebi	rs35461710
HLI	rs35461710
Exac	rs35461710
Gnomad	rs35461710
Varsome	rs35461710
LitVar	rs35461710
Map	rs35461710
PheGenI	rs35461710
Biobank	rs35461710
1000 genomes	rs35461710
hgdp	rs35461710
ensembl	rs35461710
geneview	rs35461710
scholar	rs35461710
google	rs35461710
pharmgkb	rs35461710
gwascentral	rs35461710
openSNP	rs35461710
23andMe	rs35461710
SNPshot	rs35461710
SNPdbe	rs35461710
MSV3d	rs35461710
GWAS Ctlg	rs35461710

Max Magnitude

0

OMIM	141900
Desc
Variant	0288
Related	also

ClinVar
Risk	rs35461710(T;T)
Alt	rs35461710(T;T)
Reference	Rs35461710(C;C)
Significance	Other
Disease	HEMOGLOBIN TUNIS
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN TUNIS
Reversed	1
HGVS	NC_000011.9:g.5246899G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016631.2,

[PMID 3384695] Hb Tunis [alpha 2 beta 2 124 (H2)Pro----Ser], a new beta chain variant identified by HPLC.