rs35239527

Orientation

plus

Stabilized

plus

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

Make rs35239527(G;T)

Make rs35239527(T;T)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177098

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs35239527
dbSNP (classic)	rs35239527
ClinGen	rs35239527
ebi	rs35239527
HLI	rs35239527
Exac	rs35239527
Gnomad	rs35239527
Varsome	rs35239527
LitVar	rs35239527
Map	rs35239527
PheGenI	rs35239527
Biobank	rs35239527
1000 genomes	rs35239527
hgdp	rs35239527
ensembl	rs35239527
geneview	rs35239527
scholar	rs35239527
google	rs35239527
pharmgkb	rs35239527
gwascentral	rs35239527
openSNP	rs35239527
23andMe	rs35239527
SNPshot	rs35239527
SNPdbe	rs35239527
MSV3d	rs35239527
GWAS Ctlg	rs35239527

Max Magnitude

0

OMIM	141800
Desc
Variant	0090
Related	also

ClinVar
Risk	rs35239527(T;T)
Alt	rs35239527(T;T)
Reference	Rs35239527(G;G)
Significance	Other
Disease	HEMOGLOBIN LOIRE
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN LOIRE
Reversed	0
HGVS	NC_000016.9:g.227097G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017096.2,

[PMID 3142772] Increased oxygen affinity with normal heterotropic effects in hemoglobin Loire [alpha 88(F9)Ala----Ser].