rs34608326

Orientation

plus

Stabilized

plus

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

Make rs34608326(A;A)

Make rs34608326(A;G)

Reference

GRCh38 38.1/141

Chromosome

16

Position

176784

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs34608326
dbSNP (classic)	rs34608326
ClinGen	rs34608326
ebi	rs34608326
HLI	rs34608326
Exac	rs34608326
Gnomad	rs34608326
Varsome	rs34608326
LitVar	rs34608326
Map	rs34608326
PheGenI	rs34608326
Biobank	rs34608326
1000 genomes	rs34608326
hgdp	rs34608326
ensembl	rs34608326
geneview	rs34608326
scholar	rs34608326
google	rs34608326
pharmgkb	rs34608326
gwascentral	rs34608326
openSNP	rs34608326
23andMe	rs34608326
SNPshot	rs34608326
SNPdbe	rs34608326
MSV3d	rs34608326
GWAS Ctlg	rs34608326

Max Magnitude

0

OMIM	141800
Desc
Variant	0067
Related	also

ClinVar
Risk	rs34608326(A;A)
Alt	rs34608326(A;A)
Reference	Rs34608326(G;G)
Significance	Other
Disease	HEMOGLOBIN J (MEDELLIN)
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN J (MEDELLIN)
Reversed	0
HGVS	NC_000016.9:g.226783G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017066.2,