rs35278874

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs35278874(C;G)

Make rs35278874(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5226718

Gene

HBB

is a	snp
is	mentioned by
dbSNP	rs35278874
dbSNP (classic)	rs35278874
ClinGen	rs35278874
ebi	rs35278874
HLI	rs35278874
Exac	rs35278874
Gnomad	rs35278874
Varsome	rs35278874
LitVar	rs35278874
Map	rs35278874
PheGenI	rs35278874
Biobank	rs35278874
1000 genomes	rs35278874
hgdp	rs35278874
ensembl	rs35278874
geneview	rs35278874
scholar	rs35278874
google	rs35278874
pharmgkb	rs35278874
gwascentral	rs35278874
openSNP	rs35278874
23andMe	rs35278874
SNPshot	rs35278874
SNPdbe	rs35278874
MSV3d	rs35278874
GWAS Ctlg	rs35278874

Max Magnitude

0

OMIM	141900
Desc
Variant	0082
Related	also

ClinVar
Risk	rs35278874(A;A) rs35278874(G;G) rs35278874(T;T)
Alt	rs35278874(A;A) rs35278874(G;G) rs35278874(T;T)
Reference	Rs35278874(C;C)
Significance	Other
Disease	HEMOGLOBIN G (FERRARA)
Variation	info
Gene	HBB
CLNDBN	HEMOGLOBIN G (FERRARA)
Reversed	1
HGVS	NC_000011.9:g.5247948G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016347.2,

[PMID 26414] Properties of hemoglobin G. Ferrara (beta57(E1) Asn replaced by Lys).