rs33910377

Orientation

plus

Stabilized

plus

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

Make rs33910377(C;G)

Make rs33910377(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177326

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs33910377
dbSNP (classic)	rs33910377
ClinGen	rs33910377
ebi	rs33910377
HLI	rs33910377
Exac	rs33910377
Gnomad	rs33910377
Varsome	rs33910377
LitVar	rs33910377
Map	rs33910377
PheGenI	rs33910377
Biobank	rs33910377
1000 genomes	rs33910377
hgdp	rs33910377
ensembl	rs33910377
geneview	rs33910377
scholar	rs33910377
google	rs33910377
pharmgkb	rs33910377
gwascentral	rs33910377
openSNP	rs33910377
23andMe	rs33910377
SNPshot	rs33910377
SNPdbe	rs33910377
MSV3d	rs33910377
GWAS Ctlg	rs33910377

Max Magnitude

0

OMIM	141800
Desc
Variant	0019
Related	also

OMIM	141800
Desc
Variant	0108
Related	also

ClinVar
Risk	rs33910377(G;G) rs33910377(T;T)
Alt	rs33910377(G;G) rs33910377(T;T)
Reference	Rs33910377(C;C)
Significance	Other
Disease	HEMOGLOBIN CHIAPAS HEMOGLOBIN NOUAKCHOTT
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN CHIAPAS HEMOGLOBIN NOUAKCHOTT
Reversed	0
HGVS	NC_000016.9:g.227325C>G; NC_000016.9:g.227325C>T
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017006.2, RCV000017125.2,

[PMID 5650416] Chemical characterization of hemoglobin-Mexico and hemoglobin-Chiapas.

[PMID 7319830] Hb Chiapas alpha 2 114 Pro replaced by Arg beta 2: identification by high pressure liquid chromatography.

[PMID 2790052] Hemoglobin Nouakchott [alpha 114(GH2)Pro----Leu]: a new hemoglobin variant displaying an unusual increase in hydrophobicity.