rs34915311

Orientation

minus

Stabilized

minus

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

Make rs34915311(G;G)

Make rs34915311(G;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5254440

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs34915311
dbSNP (classic)	rs34915311
ClinGen	rs34915311
ebi	rs34915311
HLI	rs34915311
Exac	rs34915311
Gnomad	rs34915311
Varsome	rs34915311
LitVar	rs34915311
Map	rs34915311
PheGenI	rs34915311
Biobank	rs34915311
1000 genomes	rs34915311
hgdp	rs34915311
ensembl	rs34915311
geneview	rs34915311
scholar	rs34915311
google	rs34915311
pharmgkb	rs34915311
gwascentral	rs34915311
openSNP	rs34915311
23andMe	rs34915311
SNPshot	rs34915311
SNPdbe	rs34915311
MSV3d	rs34915311
GWAS Ctlg	rs34915311

Max Magnitude

0

OMIM	142250
Desc
Variant	0010
Related	also

ClinVar
Risk	rs34915311(G;G)
Alt	rs34915311(G;G)
Reference	Rs34915311(T;T)
Significance	Other
Disease	HEMOGLOBIN F (KINGSTON)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (KINGSTON)
Reversed	1
HGVS	NC_000011.9:g.5275670A>C
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016106.1,

[PMID 2448270] Hb F-Kingston or alpha 2G gamma 2(55)(D6)Met----Arg in a Spanish newborn.

[PMID 6186522] Hb F Kingston (G gamma 55 [D6] Met leads to Arg).