rs35746147

Orientation

minus

Stabilized

minus

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

Make rs35746147(A;A)

Make rs35746147(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5249522

Gene

HBG1

is a	snp
is	mentioned by
dbSNP	rs35746147
dbSNP (classic)	rs35746147
ClinGen	rs35746147
ebi	rs35746147
HLI	rs35746147
Exac	rs35746147
Gnomad	rs35746147
Varsome	rs35746147
LitVar	rs35746147
Map	rs35746147
PheGenI	rs35746147
Biobank	rs35746147
1000 genomes	rs35746147
hgdp	rs35746147
ensembl	rs35746147
geneview	rs35746147
scholar	rs35746147
google	rs35746147
pharmgkb	rs35746147
gwascentral	rs35746147
openSNP	rs35746147
23andMe	rs35746147
SNPshot	rs35746147
SNPdbe	rs35746147
MSV3d	rs35746147
GWAS Ctlg	rs35746147

Max Magnitude

0

OMIM	142200
Desc
Variant	0003
Related	also

ClinVar
Risk	rs35746147(A;A)
Alt	rs35746147(A;A)
Reference	Rs35746147(C;C)
Significance	Other
Disease	HEMOGLOBIN F (BEECH ISLAND)
Variation	info
Gene	HBG1
CLNDBN	HEMOGLOBIN F (BEECH ISLAND)
Reversed	1
HGVS	NC_000011.9:g.5270752G>T
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000016147.1,

[PMID 2417989] Hb F-Beech Island or alpha 2A gamma 2(53)(D4)Ala----Asp.