rs34703519

Orientation

minus

Stabilized

minus

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

Make rs34703519(A;C)

Make rs34703519(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5253360

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs34703519
dbSNP (classic)	rs34703519
ClinGen	rs34703519
ebi	rs34703519
HLI	rs34703519
Exac	rs34703519
Gnomad	rs34703519
Varsome	rs34703519
LitVar	rs34703519
Map	rs34703519
PheGenI	rs34703519
Biobank	rs34703519
1000 genomes	rs34703519
hgdp	rs34703519
ensembl	rs34703519
geneview	rs34703519
scholar	rs34703519
google	rs34703519
pharmgkb	rs34703519
gwascentral	rs34703519
openSNP	rs34703519
23andMe	rs34703519
SNPshot	rs34703519
SNPdbe	rs34703519
MSV3d	rs34703519
GWAS Ctlg	rs34703519

Max Magnitude

0

OMIM	142250
Desc
Variant	0003
Related	also

ClinVar
Risk	rs34703519(C;C)
Alt	rs34703519(C;C)
Reference	Rs34703519(A;A)
Significance	Other
Disease	HEMOGLOBIN F (CALTECH)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (CALTECH)
Reversed	1
HGVS	NC_000011.9:g.5274590T>G
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016099.1,

[PMID 6186635] Hemoglobin F-Caltech: alpha 2 G gamma 2 120Lys replaced by Gln.