rs34823698

plus

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

Make rs34823698(A;G)

Make rs34823698(G;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177038

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs34823698
dbSNP (classic)	rs34823698
ClinGen	rs34823698
ebi	rs34823698
HLI	rs34823698
Exac	rs34823698
Gnomad	rs34823698
Varsome	rs34823698
LitVar	rs34823698
Map	rs34823698
PheGenI	rs34823698
Biobank	rs34823698
1000 genomes	rs34823698
hgdp	rs34823698
ensembl	rs34823698
geneview	rs34823698
scholar	rs34823698
google	rs34823698
pharmgkb	rs34823698
gwascentral	rs34823698
openSNP	rs34823698
23andMe	rs34823698
SNPshot	rs34823698
SNPdbe	rs34823698
MSV3d	rs34823698
GWAS Ctlg	rs34823698

Max Magnitude

0

OMIM	141800
Desc
Variant	0154
Related	also

ClinVar
Risk	rs34823698(C;C) rs34823698(G;G) rs34823698(T;T)
Alt	rs34823698(C;C) rs34823698(G;G) rs34823698(T;T)
Reference	Rs34823698(A;A)
Significance	Other
Disease	HEMOGLOBIN UBE-2
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN UBE-2
Reversed	0
HGVS	NC_000016.9:g.227037A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017176.2,

[PMID 5416123] Studies on the function of abnormal hemoglobins. II. Oxygen equilibrium of abnormal hemoglobins: Shimonoseki, Ube II, Hikari, Gifu, and Agenogi.

[PMID 6035181] Amino acid substitution of hemoglobin Ube 2 (alpha-2 68asp beta-2): an example of successful application of partial hydrolysis of peptide with 5 per cent acetic acid.

[PMID 11939522] Hb Ube-2 in a Taiwanese subject: an A-->G substitution at codon 68 of the alpha2-globin gene.

[PMID 18473246] Hb Jeddah [alpha68(E17)Asn-->His (alpha1)]: a newly recognized alpha chain variant, seen in combination with Hb S [beta6(A3)Glu-->Val], and found in three separate families of middle eastern origin.