rs34879587

Orientation

plus

Stabilized

plus

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

Make rs34879587(A;A)

Make rs34879587(A;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177081

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs34879587
dbSNP (classic)	rs34879587
ClinGen	rs34879587
ebi	rs34879587
HLI	rs34879587
Exac	rs34879587
Gnomad	rs34879587
Varsome	rs34879587
LitVar	rs34879587
Map	rs34879587
PheGenI	rs34879587
Biobank	rs34879587
1000 genomes	rs34879587
hgdp	rs34879587
ensembl	rs34879587
geneview	rs34879587
scholar	rs34879587
google	rs34879587
pharmgkb	rs34879587
gwascentral	rs34879587
openSNP	rs34879587
23andMe	rs34879587
SNPshot	rs34879587
SNPdbe	rs34879587
MSV3d	rs34879587
GWAS Ctlg	rs34879587

Max Magnitude

0

OMIM	141800
Desc
Variant	0044
Related	also

ClinVar
Risk	rs34879587(A;A)
Alt	rs34879587(A;A)
Reference	Rs34879587(C;C)
Significance	Other
Disease	HEMOGLOBIN GARDEN STATE
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN GARDEN STATE
Reversed	0
HGVS	NC_000016.9:g.227080C>A
CLNSRC	HBVAR OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017036.2,