rs35521813

Orientation

minus

Stabilized

minus

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

Make rs35521813(A;C)

Make rs35521813(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5254704

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs35521813
dbSNP (classic)	rs35521813
ClinGen	rs35521813
ebi	rs35521813
HLI	rs35521813
Exac	rs35521813
Gnomad	rs35521813
Varsome	rs35521813
LitVar	rs35521813
Map	rs35521813
PheGenI	rs35521813
Biobank	rs35521813
1000 genomes	rs35521813
hgdp	rs35521813
ensembl	rs35521813
geneview	rs35521813
scholar	rs35521813
google	rs35521813
pharmgkb	rs35521813
gwascentral	rs35521813
openSNP	rs35521813
23andMe	rs35521813
SNPshot	rs35521813
SNPdbe	rs35521813
MSV3d	rs35521813
GWAS Ctlg	rs35521813

Max Magnitude

0

OMIM	142250
Desc
Variant	0001
Related	also

ClinVar
Risk	rs35521813(C;C) rs35521813(G;G)
Alt	rs35521813(C;C) rs35521813(G;G)
Reference	Rs35521813(A;A)
Significance	Other
Disease	HEMOGLOBIN F (ALBAICIN)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (ALBAICIN)
Reversed	1
HGVS	NC_000011.9:g.5275934T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016097.2,

[PMID 2435680] Hb F-Albaicin or G gamma 8(A5)Lys----Glu or Gln.