rs34263826

Orientation

minus

Stabilized

minus

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

Make rs34263826(A;G)

Make rs34263826(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5254712

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs34263826
dbSNP (classic)	rs34263826
ClinGen	rs34263826
ebi	rs34263826
HLI	rs34263826
Exac	rs34263826
Gnomad	rs34263826
Varsome	rs34263826
LitVar	rs34263826
Map	rs34263826
PheGenI	rs34263826
Biobank	rs34263826
1000 genomes	rs34263826
hgdp	rs34263826
ensembl	rs34263826
geneview	rs34263826
scholar	rs34263826
google	rs34263826
pharmgkb	rs34263826
gwascentral	rs34263826
openSNP	rs34263826
23andMe	rs34263826
SNPshot	rs34263826
SNPdbe	rs34263826
MSV3d	rs34263826
GWAS Ctlg	rs34263826

Max Magnitude

0

OMIM	142200
Desc
Variant	0014
Related	also

OMIM	142250
Desc
Variant	0016
Related	also

ClinVar
Risk	rs34263826(G;G)
Alt	rs34263826(G;G)
Reference	Rs34263826(A;A)
Significance	Other
Disease	HEMOGLOBIN F (MEINOHAMA)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (MEINOHAMA)
Reversed	1
HGVS	NC_000011.9:g.5275942T>C
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016112.1,

[PMID 6172403] Hb F-Meinohama or alpha 2 gamma 2 (5 Glu replaced by Gly; 75 Ile; 136 Gly).