rs35957832

Orientation

minus

Stabilized

minus

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

Make rs35957832(C;C)

Make rs35957832(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5249729

Gene

HBG1

is a	snp
is	mentioned by
dbSNP	rs35957832
dbSNP (classic)	rs35957832
ClinGen	rs35957832
ebi	rs35957832
HLI	rs35957832
Exac	rs35957832
Gnomad	rs35957832
Varsome	rs35957832
LitVar	rs35957832
Map	rs35957832
PheGenI	rs35957832
Biobank	rs35957832
1000 genomes	rs35957832
hgdp	rs35957832
ensembl	rs35957832
geneview	rs35957832
scholar	rs35957832
google	rs35957832
pharmgkb	rs35957832
gwascentral	rs35957832
openSNP	rs35957832
23andMe	rs35957832
SNPshot	rs35957832
SNPdbe	rs35957832
MSV3d	rs35957832
GWAS Ctlg	rs35957832

Max Magnitude

0

OMIM	142200
Desc
Variant	0022
Related	also

ClinVar
Risk	rs35957832(C;C)
Alt	rs35957832(C;C)
Reference	Rs35957832(G;G)
Significance	Other
Disease	HEMOGLOBIN F (XINJIANG)
Variation	info
Gene	HBG1
CLNDBN	HEMOGLOBIN F (XINJIANG)
Reversed	1
HGVS	NC_000011.9:g.5270959C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016167.3,

[PMID 2448268] Hb F-Xinjiang or A gamma T25(B7)Gly----Arg: a new slow-moving unstable fetal hemoglobin variant.