rs33996798

Orientation

plus

Stabilized

plus

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

Make rs33996798(C;G)

Make rs33996798(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177088

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs33996798
dbSNP (classic)	rs33996798
ClinGen	rs33996798
ebi	rs33996798
HLI	rs33996798
Exac	rs33996798
Gnomad	rs33996798
Varsome	rs33996798
LitVar	rs33996798
Map	rs33996798
PheGenI	rs33996798
Biobank	rs33996798
1000 genomes	rs33996798
hgdp	rs33996798
ensembl	rs33996798
geneview	rs33996798
scholar	rs33996798
google	rs33996798
pharmgkb	rs33996798
gwascentral	rs33996798
openSNP	rs33996798
23andMe	rs33996798
SNPshot	rs33996798
SNPdbe	rs33996798
MSV3d	rs33996798
GWAS Ctlg	rs33996798

Max Magnitude

0

OMIM	141800
Desc
Variant	0030
Related	also

ClinVar
Risk	rs33996798(A;A) rs33996798(G;G)
Alt	rs33996798(A;A) rs33996798(G;G)
Reference	Rs33996798(C;C)
Significance	Untested
Disease
Variation	info
Gene	HBA1
CLNDBN
Reversed	0
HGVS	NC_000016.9:g.227087C>A; NC_000016.9:g.227087C>G
CLNSRC
CLNACC

[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.