rs34532478

Orientation

minus

Stabilized

minus

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

Make rs34532478(A;G)

Make rs34532478(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5254486

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs34532478
dbSNP (classic)	rs34532478
ClinGen	rs34532478
ebi	rs34532478
HLI	rs34532478
Exac	rs34532478
Gnomad	rs34532478
Varsome	rs34532478
LitVar	rs34532478
Map	rs34532478
PheGenI	rs34532478
Biobank	rs34532478
1000 genomes	rs34532478
hgdp	rs34532478
ensembl	rs34532478
geneview	rs34532478
scholar	rs34532478
google	rs34532478
pharmgkb	rs34532478
gwascentral	rs34532478
openSNP	rs34532478
23andMe	rs34532478
SNPshot	rs34532478
SNPdbe	rs34532478
MSV3d	rs34532478
GWAS Ctlg	rs34532478

Max Magnitude

0

OMIM	142250
Desc
Variant	0044
Related	also

ClinVar
Risk	rs34532478(G;G)
Alt	rs34532478(G;G)
Reference	Rs34532478(A;A)
Significance	Other
Disease	HEMOGLOBIN F (VELETA)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (VELETA)
Reversed	1
HGVS	NC_000011.9:g.5275716T>C
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016139.2,

[PMID 8718700] Hb F-Veleta or alpha 2 G gamma(2)40(C6)Arg-->Gly.