rs34150306

Orientation

minus

Stabilized

minus

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

Make rs34150306(A;G)

Make rs34150306(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5254374

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs34150306
dbSNP (classic)	rs34150306
ClinGen	rs34150306
ebi	rs34150306
HLI	rs34150306
Exac	rs34150306
Gnomad	rs34150306
Varsome	rs34150306
LitVar	rs34150306
Map	rs34150306
PheGenI	rs34150306
Biobank	rs34150306
1000 genomes	rs34150306
hgdp	rs34150306
ensembl	rs34150306
geneview	rs34150306
scholar	rs34150306
google	rs34150306
pharmgkb	rs34150306
gwascentral	rs34150306
openSNP	rs34150306
23andMe	rs34150306
SNPshot	rs34150306
SNPdbe	rs34150306
MSV3d	rs34150306
GWAS Ctlg	rs34150306

Max Magnitude

0

OMIM	142250
Desc
Variant	0009
Related	also

ClinVar
Risk	rs34150306(G;G) rs34150306(T;T)
Alt	rs34150306(G;G) rs34150306(T;T)
Reference	Rs34150306(A;A)
Significance	Other
Disease	HEMOGLOBIN F (KENNESTONE)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (KENNESTONE)
Reversed	1
HGVS	NC_000011.9:g.5275604T>C
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016105.1,

[PMID 6192110] Hb F-Kennestone or alpha 2G gamma 2 (EF1)77 His leads to Arg observed in a Caucasian baby.