rs33926206

Orientation

plus

Stabilized

plus

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

Make rs33926206(A;C)

Make rs33926206(C;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177086

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs33926206
dbSNP (classic)	rs33926206
ClinGen	rs33926206
ebi	rs33926206
HLI	rs33926206
Exac	rs33926206
Gnomad	rs33926206
Varsome	rs33926206
LitVar	rs33926206
Map	rs33926206
PheGenI	rs33926206
Biobank	rs33926206
1000 genomes	rs33926206
hgdp	rs33926206
ensembl	rs33926206
geneview	rs33926206
scholar	rs33926206
google	rs33926206
pharmgkb	rs33926206
gwascentral	rs33926206
openSNP	rs33926206
23andMe	rs33926206
SNPshot	rs33926206
SNPdbe	rs33926206
MSV3d	rs33926206
GWAS Ctlg	rs33926206

Max Magnitude

0

OMIM	141800
Desc
Variant	0030
Related	also

ClinVar
Risk	rs33926206(C;C) rs33926206(G;G)
Alt	rs33926206(C;C) rs33926206(G;G)
Reference	Rs33926206(A;A)
Significance	Other
Disease	HEMOGLOBIN ETOBICOKE
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN ETOBICOKE
Reversed	0
HGVS	NC_000016.9:g.227085A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017017.2,

[PMID 5774804] Hemoglobin Etobicoke: alpha-84(F5) serine replaced by arginine.

[PMID 6874377] Hb Etobicoke, alpha 85(F5) Ser leads to Arg found in a newborn of French-Indian-English descent.