rs63750122

Orientation

plus

Stabilized

plus

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

Make rs63750122(-;-)

Make rs63750122(-;TCTGCCCAGGTTAAGGGCCACGGC)

Reference

GRCh38 38.1/141

Chromosome

16

Position

176990

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs63750122
dbSNP (classic)	rs63750122
ClinGen	rs63750122
ebi	rs63750122
HLI	rs63750122
Exac	rs63750122
Gnomad	rs63750122
Varsome	rs63750122
LitVar	rs63750122
Map	rs63750122
PheGenI	rs63750122
Biobank	rs63750122
1000 genomes	rs63750122
hgdp	rs63750122
ensembl	rs63750122
geneview	rs63750122
scholar	rs63750122
google	rs63750122
pharmgkb	rs63750122
gwascentral	rs63750122
openSNP	rs63750122
23andMe	rs63750122
SNPshot	rs63750122
SNPdbe	rs63750122
MSV3d	rs63750122
GWAS Ctlg	rs63750122

Max Magnitude

0

OMIM	141800
Desc
Variant	0199
Related	also

ClinVar
Risk	rs63750122(-;-)
Alt	rs63750122(-;-)
Reference	rs63750122(GCCACGGCTCTGCCCAGGTTAAGG;GCCACGGCTCTGCCCAGGTTAAGG)
Significance	Other
Disease	HEMOGLOBIN J (BISKRA)
Variation	info
Gene	HBA1
CLNDBN	HEMOGLOBIN J (BISKRA)
Reversed	0
HGVS	NC_000016.9:g.226989_227012del24
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017218.2,