rs35812514

Orientation

minus

Stabilized

minus

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

Make rs35812514(A;A)

Make rs35812514(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5254324

Gene

HBG2

is a	snp
is	mentioned by
dbSNP	rs35812514
dbSNP (classic)	rs35812514
ClinGen	rs35812514
ebi	rs35812514
HLI	rs35812514
Exac	rs35812514
Gnomad	rs35812514
Varsome	rs35812514
LitVar	rs35812514
Map	rs35812514
PheGenI	rs35812514
Biobank	rs35812514
1000 genomes	rs35812514
hgdp	rs35812514
ensembl	rs35812514
geneview	rs35812514
scholar	rs35812514
google	rs35812514
pharmgkb	rs35812514
gwascentral	rs35812514
openSNP	rs35812514
23andMe	rs35812514
SNPshot	rs35812514
SNPdbe	rs35812514
MSV3d	rs35812514
GWAS Ctlg	rs35812514

Max Magnitude

0

OMIM	142250
Desc
Variant	0006
Related	also

ClinVar
Risk	rs35812514(A;A)
Alt	rs35812514(A;A)
Reference	Rs35812514(G;G)
Significance	Other
Disease	HEMOGLOBIN F (COLUMBUS-GA)
Variation	info
Gene	HBG2
CLNDBN	HEMOGLOBIN F (COLUMBUS-GA)
Reversed	1
HGVS	NC_000011.9:g.5275554C>T
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000016102.1,

[PMID 6186636] Hb F-Columbus-Ga or alpha 2 G gamma 2 94(FGl) Asp replaced by Asn.