rs35252931

Orientation

plus

Stabilized

plus

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

Make rs35252931(C;C)

Make rs35252931(C;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177005

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs35252931
dbSNP (classic)	rs35252931
ClinGen	rs35252931
ebi	rs35252931
HLI	rs35252931
Exac	rs35252931
Gnomad	rs35252931
Varsome	rs35252931
LitVar	rs35252931
Map	rs35252931
PheGenI	rs35252931
Biobank	rs35252931
1000 genomes	rs35252931
hgdp	rs35252931
ensembl	rs35252931
geneview	rs35252931
scholar	rs35252931
google	rs35252931
pharmgkb	rs35252931
gwascentral	rs35252931
openSNP	rs35252931
23andMe	rs35252931
SNPshot	rs35252931
SNPdbe	rs35252931
MSV3d	rs35252931
GWAS Ctlg	rs35252931

Max Magnitude

0

OMIM	141800
Desc
Variant	0086
Related	also

ClinVar
Risk	rs35252931(C;C)
Alt	rs35252931(C;C)
Reference	Rs35252931(G;G)
Significance	Other
Disease	HEMOGLOBIN L (PERSIAN GULF)
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN L (PERSIAN GULF)
Reversed	0
HGVS	NC_000016.9:g.227004G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017092.2,

[PMID 4982774] Haemoglobin L Persian Gulf: alpha-57 (E6) glycine leads to arginine.