rs35960772

Orientation

minus

Stabilized

minus

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

Make rs35960772(A;G)

Make rs35960772(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226639

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs35960772
dbSNP (classic)	rs35960772
ClinGen	rs35960772
ebi	rs35960772
HLI	rs35960772
Exac	rs35960772
Gnomad	rs35960772
Varsome	rs35960772
LitVar	rs35960772
Map	rs35960772
PheGenI	rs35960772
Biobank	rs35960772
1000 genomes	rs35960772
hgdp	rs35960772
ensembl	rs35960772
geneview	rs35960772
scholar	rs35960772
google	rs35960772
pharmgkb	rs35960772
gwascentral	rs35960772
openSNP	rs35960772
23andMe	rs35960772
SNPshot	rs35960772
SNPdbe	rs35960772
MSV3d	rs35960772
GWAS Ctlg	rs35960772

Max Magnitude

0

OMIM	141900
Desc
Variant	0491
Related	also

ClinVar
Risk	rs35960772(G;G)
Alt	rs35960772(G;G)
Reference	Rs35960772(A;A)
Significance	Other
Disease	HEMOGLOBIN SAALE
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN SAALE
Reversed	1
HGVS	NC_000011.9:g.5247869T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016846.2,

[PMID 10770934] Characterization of a new electrophoretically silent hemoglobin variant. Hb saale OR alpha 2beta 2 84(EF8)Thr --> Ala.