rs35993097

Orientation

plus

Stabilized

plus

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

Make rs35993097(A;A)

Make rs35993097(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

176772

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs35993097
dbSNP (classic)	rs35993097
ClinGen	rs35993097
ebi	rs35993097
HLI	rs35993097
Exac	rs35993097
Gnomad	rs35993097
Varsome	rs35993097
LitVar	rs35993097
Map	rs35993097
PheGenI	rs35993097
Biobank	rs35993097
1000 genomes	rs35993097
hgdp	rs35993097
ensembl	rs35993097
geneview	rs35993097
scholar	rs35993097
google	rs35993097
pharmgkb	rs35993097
gwascentral	rs35993097
openSNP	rs35993097
23andMe	rs35993097
SNPshot	rs35993097
SNPdbe	rs35993097
MSV3d	rs35993097
GWAS Ctlg	rs35993097

Max Magnitude

0

OMIM	141800
Desc
Variant	0175
Related	also

ClinVar
Risk	rs35993097(A;A)
Alt	rs35993097(A;A)
Reference	Rs35993097(G;G)
Significance	Other
Disease	HEMOGLOBIN AL-AIN ABU DHABI
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN AL-AIN ABU DHABI
Reversed	0
HGVS	NC_000016.9:g.226771G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017195.2,

[PMID 1428941] HB Al-Ain Abu Dhabi [alpha 18(A16)Gly----Asp]: a new hemoglobin variant discovered in an Emiratee family.