rs34997902

Orientation

minus

Stabilized

minus

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

Make rs34997902(A;C)

Make rs34997902(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5253344

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs34997902
dbSNP (classic)	rs34997902
ClinGen	rs34997902
ebi	rs34997902
HLI	rs34997902
Exac	rs34997902
Gnomad	rs34997902
Varsome	rs34997902
LitVar	rs34997902
Map	rs34997902
PheGenI	rs34997902
Biobank	rs34997902
1000 genomes	rs34997902
hgdp	rs34997902
ensembl	rs34997902
geneview	rs34997902
scholar	rs34997902
google	rs34997902
pharmgkb	rs34997902
gwascentral	rs34997902
openSNP	rs34997902
23andMe	rs34997902
SNPshot	rs34997902
SNPdbe	rs34997902
MSV3d	rs34997902
GWAS Ctlg	rs34997902

Max Magnitude

0

OMIM	142250
Desc
Variant	0021
Related	also

ClinVar
Risk	rs34997902(C;C) rs34997902(T;T)
Alt	rs34997902(C;C) rs34997902(T;T)
Reference	Rs34997902(A;A)
Significance	Other
Disease	HEMOGLOBIN F (PORT ROYAL)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (PORT ROYAL)
Reversed	1
HGVS	NC_000011.9:g.5274574T>G
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016117.1,

[PMID 4846278] Haemoglobin F Port Royal (alpha2G gamma2 125 Glu leads to Ala).