rs41514946

Orientation

plus

Stabilized

plus

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

Make rs41514946(A;A)

Make rs41514946(A;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

173573

Gene

HBA2

is a	snp
is	mentioned by
dbSNP	rs41514946
dbSNP (classic)	rs41514946
ClinGen	rs41514946
ebi	rs41514946
HLI	rs41514946
Exac	rs41514946
Gnomad	rs41514946
Varsome	rs41514946
LitVar	rs41514946
Map	rs41514946
PheGenI	rs41514946
Biobank	rs41514946
1000 genomes	rs41514946
hgdp	rs41514946
ensembl	rs41514946
geneview	rs41514946
scholar	rs41514946
google	rs41514946
pharmgkb	rs41514946
gwascentral	rs41514946
openSNP	rs41514946
23andMe	rs41514946
SNPshot	rs41514946
SNPdbe	rs41514946
MSV3d	rs41514946
GWAS Ctlg	rs41514946

Max Magnitude

0

OMIM	141850
Desc
Variant	0062
Related	also

ClinVar
Risk	rs41514946(A;A) rs41514946(G;G)
Alt	rs41514946(A;A) rs41514946(G;G)
Reference	Rs41514946(C;C)
Significance	Other
Disease	Hemoglobin Val de Marne
Variation	info
Gene	HBA2
CLNDBN	Hemoglobin Val de Marne
Reversed	0
HGVS	NC_000016.9:g.223572C>A
CLNSRC	HBVAR OMIM Allelic Variant
CLNACC	RCV000016974.2,