rs397514502

Orientation

minus

Stabilized

minus

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

Make rs397514502(C;G)

Make rs397514502(G;G)

Reference

GRCh38 38.1/141

Chromosome

22

Position

42693321

Gene

A4GALT

is a	snp
is	mentioned by
dbSNP	rs397514502
dbSNP (classic)	rs397514502
ClinGen	rs397514502
ebi	rs397514502
HLI	rs397514502
Exac	rs397514502
Gnomad	rs397514502
Varsome	rs397514502
LitVar	rs397514502
Map	rs397514502
PheGenI	rs397514502
Biobank	rs397514502
1000 genomes	rs397514502
hgdp	rs397514502
ensembl	rs397514502
geneview	rs397514502
scholar	rs397514502
google	rs397514502
pharmgkb	rs397514502
gwascentral	rs397514502
openSNP	rs397514502
23andMe	rs397514502
SNPshot	rs397514502
SNPdbe	rs397514502
MSV3d	rs397514502
GWAS Ctlg	rs397514502

Max Magnitude

0

ClinVar
Risk	rs397514502(G;G)
Alt	rs397514502(G;G)
Reference	Rs397514502(C;C)
Significance	Other
Disease	p phenotype
Variation	info
Gene	A4GALT
CLNDBN	p phenotype
Reversed	1
HGVS	NC_000022.10:g.43089327G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000032632.3,