rs63750679

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs63750679(A;A)

Make rs63750679(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

172968

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs63750679
dbSNP (classic)	rs63750679
ClinGen	rs63750679
ebi	rs63750679
HLI	rs63750679
Exac	rs63750679
Gnomad	rs63750679
Varsome	rs63750679
LitVar	rs63750679
Map	rs63750679
PheGenI	rs63750679
Biobank	rs63750679
1000 genomes	rs63750679
hgdp	rs63750679
ensembl	rs63750679
geneview	rs63750679
scholar	rs63750679
google	rs63750679
pharmgkb	rs63750679
gwascentral	rs63750679
openSNP	rs63750679
23andMe	rs63750679
SNPshot	rs63750679
SNPdbe	rs63750679
MSV3d	rs63750679
GWAS Ctlg	rs63750679

Max Magnitude

0

OMIM	141800
Desc
Variant	0175
Related	also

ClinVar
Risk	rs63750679(A;A)
Alt	rs63750679(A;A)
Reference	Rs63750679(G;G)
Significance	Untested
Disease
Variation	info
Gene	HBA2
CLNDBN
Reversed	0
HGVS	NC_000016.9:g.222967G>A
CLNSRC
CLNACC

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