rs74315453

Orientation

minus

Stabilized

minus

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

Make rs74315453(A;A)

Make rs74315453(A;T)

Reference

GRCh38 38.1/141

Chromosome

22

Position

42693404

Gene

A4GALT

is a	snp
is	mentioned by
dbSNP	rs74315453
dbSNP (classic)	rs74315453
ClinGen	rs74315453
ebi	rs74315453
HLI	rs74315453
Exac	rs74315453
Gnomad	rs74315453
Varsome	rs74315453
LitVar	rs74315453
Map	rs74315453
PheGenI	rs74315453
Biobank	rs74315453
1000 genomes	rs74315453
hgdp	rs74315453
ensembl	rs74315453
geneview	rs74315453
scholar	rs74315453
google	rs74315453
pharmgkb	rs74315453
gwascentral	rs74315453
openSNP	rs74315453
23andMe	rs74315453
SNPshot	rs74315453
SNPdbe	rs74315453
MSV3d	rs74315453
GWAS Ctlg	rs74315453

Max Magnitude

0

OMIM	607922
Desc
Variant	0001
Related	also

ClinVar
Risk	rs74315453(A;A)
Alt	rs74315453(A;A)
Reference	Rs74315453(T;T)
Significance	Other
Disease	p phenotype
Variation	info
Gene	A4GALT
CLNDBN	p phenotype
Reversed	1
HGVS	NC_000022.10:g.43089410A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002811.3,