rs35628685

Orientation

plus

Stabilized

plus

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

Make rs35628685(A;A)

Make rs35628685(A;C)

Reference

GRCh38 38.1/141

Chromosome

16

Position

176775

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs35628685
dbSNP (classic)	rs35628685
ClinGen	rs35628685
ebi	rs35628685
HLI	rs35628685
Exac	rs35628685
Gnomad	rs35628685
Varsome	rs35628685
LitVar	rs35628685
Map	rs35628685
PheGenI	rs35628685
Biobank	rs35628685
1000 genomes	rs35628685
hgdp	rs35628685
ensembl	rs35628685
geneview	rs35628685
scholar	rs35628685
google	rs35628685
pharmgkb	rs35628685
gwascentral	rs35628685
openSNP	rs35628685
23andMe	rs35628685
SNPshot	rs35628685
SNPdbe	rs35628685
MSV3d	rs35628685
GWAS Ctlg	rs35628685

Max Magnitude

0

OMIM	141800
Desc
Variant	0076
Related	also

ClinVar
Risk	rs35628685(A;A)
Alt	rs35628685(A;A)
Reference	Rs35628685(C;C)
Significance	Other
Disease	HEMOGLOBIN J (TASHIKUERGAN)
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN J (TASHIKUERGAN)
Reversed	0
HGVS	NC_000016.9:g.226774C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017074.4,

[PMID 6548207] A new fast-moving hemoglobin variant, Hb J-Tashikuergan alpha 19(AB1) Ala----Glu.