rs34019507

Orientation

minus

Stabilized

minus

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

Make rs34019507(G;T)

Make rs34019507(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5254409

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs34019507
dbSNP (classic)	rs34019507
ClinGen	rs34019507
ebi	rs34019507
HLI	rs34019507
Exac	rs34019507
Gnomad	rs34019507
Varsome	rs34019507
LitVar	rs34019507
Map	rs34019507
PheGenI	rs34019507
Biobank	rs34019507
1000 genomes	rs34019507
hgdp	rs34019507
ensembl	rs34019507
geneview	rs34019507
scholar	rs34019507
google	rs34019507
pharmgkb	rs34019507
gwascentral	rs34019507
openSNP	rs34019507
23andMe	rs34019507
SNPshot	rs34019507
SNPdbe	rs34019507
MSV3d	rs34019507
GWAS Ctlg	rs34019507

Max Magnitude

0

OMIM	142250
Desc
Variant	0005
Related	also

ClinVar
Risk	rs34019507(C;C) rs34019507(T;T)
Alt	rs34019507(C;C) rs34019507(T;T)
Reference	Rs34019507(G;G)
Significance	Other
Disease	HEMOGLOBIN F (CLARKE)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (CLARKE)
Reversed	1
HGVS	NC_000011.9:g.5275639C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016101.1,

[PMID 2442123] Hb F-Clarke or alpha 2G gamma 2(65)(E9)Lys----Asn.