rs63750388

Orientation

plus

Stabilized

plus

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

Make rs63750388(C;G)

Make rs63750388(G;G)

Reference

GRCh37 37.1/132

Chromosome

16

Position

227325

Gene

HBA1

is a	snp
is	mentioned by
dbSNP	rs63750388
dbSNP (classic)	rs63750388
ClinGen	rs63750388
ebi	rs63750388
HLI	rs63750388
Exac	rs63750388
Gnomad	rs63750388
Varsome	rs63750388
LitVar	rs63750388
Map	rs63750388
PheGenI	rs63750388
Biobank	rs63750388
1000 genomes	rs63750388
hgdp	rs63750388
ensembl	rs63750388
geneview	rs63750388
scholar	rs63750388
google	rs63750388
pharmgkb	rs63750388
gwascentral	rs63750388
openSNP	rs63750388
23andMe	rs63750388
SNPshot	rs63750388
SNPdbe	rs63750388
MSV3d	rs63750388
GWAS Ctlg	rs63750388

Status

Deleted

Max Magnitude

0

OMIM	141800
Desc
Variant	0019
Related	also

OMIM	141800
Desc
Variant	0108
Related	also

ClinVar
Risk	rs63750388(G;G) rs63750388(T;T)
Alt	rs63750388(G;G) rs63750388(T;T)
Reference	Rs63750388(C;C)
Significance	Untested
Disease
Variation	info
Gene	HBA1
CLNDBN
Reversed	0
HGVS	NC_000016.9:g.227325C>G; NC_000016.9:g.227325C>T
CLNSRC
CLNACC