rs387906280

Orientation

minus

Stabilized

minus

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

Make rs387906280(-;C)

Make rs387906280(C;C)

Reference

GRCh38 38.1/141

Chromosome

22

Position

42692922

Gene

A4GALT

is a	snp
is	mentioned by
dbSNP	rs387906280
dbSNP (classic)	rs387906280
ClinGen	rs387906280
ebi	rs387906280
HLI	rs387906280
Exac	rs387906280
Gnomad	rs387906280
Varsome	rs387906280
LitVar	rs387906280
Map	rs387906280
PheGenI	rs387906280
Biobank	rs387906280
1000 genomes	rs387906280
hgdp	rs387906280
ensembl	rs387906280
geneview	rs387906280
scholar	rs387906280
google	rs387906280
pharmgkb	rs387906280
gwascentral	rs387906280
openSNP	rs387906280
23andMe	rs387906280
SNPshot	rs387906280
SNPdbe	rs387906280
MSV3d	rs387906280
GWAS Ctlg	rs387906280

Max Magnitude

0

ClinVar
Risk	rs387906280(C;C)
Alt	rs387906280(C;C)
Reference	Rs387906280(-;-)
Significance	Other
Disease	p phenotype
Variation	info
Gene	A4GALT
CLNDBN	p phenotype
Reversed	1
HGVS	NC_000022.10:g.43088929dupG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002816.3,