rs121913127

Orientation

plus

Stabilized

plus

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

Make rs121913127(A;A)

Make rs121913127(A;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177391

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs121913127
dbSNP (classic)	rs121913127
ClinGen	rs121913127
ebi	rs121913127
HLI	rs121913127
Exac	rs121913127
Gnomad	rs121913127
Varsome	rs121913127
LitVar	rs121913127
Map	rs121913127
PheGenI	rs121913127
Biobank	rs121913127
1000 genomes	rs121913127
hgdp	rs121913127
ensembl	rs121913127
geneview	rs121913127
scholar	rs121913127
google	rs121913127
pharmgkb	rs121913127
gwascentral	rs121913127
openSNP	rs121913127
23andMe	rs121913127
SNPshot	rs121913127
SNPdbe	rs121913127
MSV3d	rs121913127
GWAS Ctlg	rs121913127

Max Magnitude

0

OMIM	141800
Desc
Variant	0020
Related	also

ClinVar
Risk	rs121913127(A;A)
Alt	rs121913127(A;A)
Reference	Rs121913127(C;C)
Significance	Other
Disease	HEMOGLOBIN CHICAGO
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN CHICAGO
Reversed	0
HGVS	NC_000016.9:g.227390C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017007.2,