rs41381645

Orientation

plus

Stabilized

plus

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

Make rs41381645(A;C)

Make rs41381645(C;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

177018

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs41381645
dbSNP (classic)	rs41381645
ClinGen	rs41381645
ebi	rs41381645
HLI	rs41381645
Exac	rs41381645
Gnomad	rs41381645
Varsome	rs41381645
LitVar	rs41381645
Map	rs41381645
PheGenI	rs41381645
Biobank	rs41381645
1000 genomes	rs41381645
hgdp	rs41381645
ensembl	rs41381645
geneview	rs41381645
scholar	rs41381645
google	rs41381645
pharmgkb	rs41381645
gwascentral	rs41381645
openSNP	rs41381645
23andMe	rs41381645
SNPshot	rs41381645
SNPdbe	rs41381645
MSV3d	rs41381645
GWAS Ctlg	rs41381645

Max Magnitude

0

OMIM	141800
Desc
Variant	0059
Related	also

ClinVar
Risk	rs41381645(C;C)
Alt	rs41381645(C;C)
Reference	Rs41381645(A;A)
Significance	Other
Disease	HEMOGLOBIN J (ANATOLIA)
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN J (ANATOLIA)
Reversed	0
HGVS	NC_000016.9:g.227017A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017058.2,

[PMID 2272835] Hb J-Anatolia [alpha 61(E10)Lys----Thr]: structural characterization and gene localization of a new alpha chain variant.