rs28940572

Orientation

minus

Stabilized

minus

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

Make rs28940572(A;A)

Make rs28940572(A;G)

Reference

GRCh38 38.1/141

Chromosome

22

Position

42693392

Gene

A4GALT

is a	snp
is	mentioned by
dbSNP	rs28940572
dbSNP (classic)	rs28940572
ClinGen	rs28940572
ebi	rs28940572
HLI	rs28940572
Exac	rs28940572
Gnomad	rs28940572
Varsome	rs28940572
LitVar	rs28940572
Map	rs28940572
PheGenI	rs28940572
Biobank	rs28940572
1000 genomes	rs28940572
hgdp	rs28940572
ensembl	rs28940572
geneview	rs28940572
scholar	rs28940572
google	rs28940572
pharmgkb	rs28940572
gwascentral	rs28940572
openSNP	rs28940572
23andMe	rs28940572
SNPshot	rs28940572
SNPdbe	rs28940572
MSV3d	rs28940572
GWAS Ctlg	rs28940572

Max Magnitude

0

OMIM	607922
Desc	P BLOOD GROUP SYSTEM, p PHENOTYPE
Variant	0004
Related	also

ClinVar
Risk	rs28940572(A;A)
Alt	rs28940572(A;A)
Reference	Rs28940572(G;G)
Significance	Other
Disease	p phenotype
Variation	info
Gene	A4GALT
CLNDBN	p phenotype
Reversed	1
HGVS	NC_000022.10:g.43089398C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002814.3,