rs35654328

Orientation

minus

Stabilized

minus

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

Make rs35654328(A;A)

Make rs35654328(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5254650

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs35654328
dbSNP (classic)	rs35654328
ClinGen	rs35654328
ebi	rs35654328
HLI	rs35654328
Exac	rs35654328
Gnomad	rs35654328
Varsome	rs35654328
LitVar	rs35654328
Map	rs35654328
PheGenI	rs35654328
Biobank	rs35654328
1000 genomes	rs35654328
hgdp	rs35654328
ensembl	rs35654328
geneview	rs35654328
scholar	rs35654328
google	rs35654328
pharmgkb	rs35654328
gwascentral	rs35654328
openSNP	rs35654328
23andMe	rs35654328
SNPshot	rs35654328
SNPdbe	rs35654328
MSV3d	rs35654328
GWAS Ctlg	rs35654328

Max Magnitude

0

OMIM	142250
Desc
Variant	0019
Related	also

ClinVar
Risk	rs35654328(A;A)
Alt	rs35654328(A;A)
Reference	Rs35654328(G;G)
Significance	Other
Disease	HEMOGLOBIN F (OAKLAND)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (OAKLAND)
Reversed	1
HGVS	NC_000011.9:g.5275880C>T
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016115.1,

[PMID 2442122] Hb F-Oakland or alpha 2G gamma I2(26)(B8)Glu----Lys.