rs28937582

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(T;T)	0

Make rs28937582(A;C)

Make rs28937582(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

161085958

Gene

B3GALNT1

is a	snp
is	mentioned by
dbSNP	rs28937582
dbSNP (classic)	rs28937582
ClinGen	rs28937582
ebi	rs28937582
HLI	rs28937582
Exac	rs28937582
Gnomad	rs28937582
Varsome	rs28937582
LitVar	rs28937582
Map	rs28937582
PheGenI	rs28937582
Biobank	rs28937582
1000 genomes	rs28937582
hgdp	rs28937582
ensembl	rs28937582
geneview	rs28937582
scholar	rs28937582
google	rs28937582
pharmgkb	rs28937582
gwascentral	rs28937582
openSNP	rs28937582
23andMe	rs28937582
SNPshot	rs28937582
SNPdbe	rs28937582
MSV3d	rs28937582
GWAS Ctlg	rs28937582

Max Magnitude

0

OMIM	603094
Desc	BLOOD GROUP--P SYSTEM, P(k) ANTIGEN
Variant	0004
Related	also

ClinVar
Risk	rs28937582(C;C)
Alt	rs28937582(C;C)
Reference	Rs28937582(A;A)
Significance	Other
Disease	p phenotype
Variation	info
Gene	B3GALNT1
CLNDBN	p phenotype
Reversed	1
HGVS	NC_000003.11:g.160803746T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007015.3,