rs35621390

Orientation

minus

Stabilized

minus

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

Make rs35621390(G;T)

Make rs35621390(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5254675

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs35621390
dbSNP (classic)	rs35621390
ClinGen	rs35621390
ebi	rs35621390
HLI	rs35621390
Exac	rs35621390
Gnomad	rs35621390
Varsome	rs35621390
LitVar	rs35621390
Map	rs35621390
PheGenI	rs35621390
Biobank	rs35621390
1000 genomes	rs35621390
hgdp	rs35621390
ensembl	rs35621390
geneview	rs35621390
scholar	rs35621390
google	rs35621390
pharmgkb	rs35621390
gwascentral	rs35621390
openSNP	rs35621390
23andMe	rs35621390
SNPshot	rs35621390
SNPdbe	rs35621390
MSV3d	rs35621390
GWAS Ctlg	rs35621390

Max Magnitude

0

OMIM	142250
Desc
Variant	0048
Related	also

ClinVar
Risk	rs35621390(C;C) rs35621390(T;T)
Alt	rs35621390(C;C) rs35621390(T;T)
Reference	Rs35621390(G;G)
Significance	Other
Disease	HEMOGLOBIN F (CLAMART)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (CLAMART)
Reversed	1
HGVS	NC_000011.9:g.5275905C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016143.3,

[PMID 10722115] Two new Ggamma chain variants: Hb F-clamart [gamma17(A14)Lys-->Asn] and Hb F-Ouled Rabah [gamma19(B1)Asn-->Lys].