rs28940571

Orientation

minus

Stabilized

minus

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

Make rs28940571(C;T)

Make rs28940571(T;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

42693200

Gene

A4GALT

is a	snp
is	mentioned by
dbSNP	rs28940571
dbSNP (classic)	rs28940571
ClinGen	rs28940571
ebi	rs28940571
HLI	rs28940571
Exac	rs28940571
Gnomad	rs28940571
Varsome	rs28940571
LitVar	rs28940571
Map	rs28940571
PheGenI	rs28940571
Biobank	rs28940571
1000 genomes	rs28940571
hgdp	rs28940571
ensembl	rs28940571
geneview	rs28940571
scholar	rs28940571
google	rs28940571
pharmgkb	rs28940571
gwascentral	rs28940571
openSNP	rs28940571
23andMe	rs28940571
SNPshot	rs28940571
SNPdbe	rs28940571
MSV3d	rs28940571
GWAS Ctlg	rs28940571

GMAF

0.0004591

Max Magnitude

0

OMIM	607922
Desc	P BLOOD GROUP SYSTEM, p PHENOTYPE
Variant	0002
Related	also

ClinVar
Risk	rs28940571(A;A) rs28940571(T;T)
Alt	rs28940571(A;A) rs28940571(T;T)
Reference	Rs28940571(C;C)
Significance	Other
Disease	p phenotype
Variation	info
Gene	A4GALT
CLNDBN	p phenotype
Reversed	1
HGVS	NC_000022.10:g.43089206G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002812.3,