rs387906279

Orientation

minus

Stabilized

minus

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

Make rs387906279(-;-)

Make rs387906279(-;CTT)

Make rs387906279(CTT;CTT)

Reference

GRCh38 38.1/141

Chromosome

22

Position

42693710

Gene

A4GALT

is a	snp
is	mentioned by
dbSNP	rs387906279
dbSNP (classic)	rs387906279
ClinGen	rs387906279
ebi	rs387906279
HLI	rs387906279
Exac	rs387906279
Gnomad	rs387906279
Varsome	rs387906279
LitVar	rs387906279
Map	rs387906279
PheGenI	rs387906279
Biobank	rs387906279
1000 genomes	rs387906279
hgdp	rs387906279
ensembl	rs387906279
geneview	rs387906279
scholar	rs387906279
google	rs387906279
pharmgkb	rs387906279
gwascentral	rs387906279
openSNP	rs387906279
23andMe	rs387906279
SNPshot	rs387906279
SNPdbe	rs387906279
MSV3d	rs387906279
GWAS Ctlg	rs387906279

Max Magnitude

0

ClinVar
Risk	Rs387906279(TTC;TTC) rs387906279(-;-)
Alt	Rs387906279(TTC;TTC) rs387906279(-;-)
Reference	rs387906279(CTT;CTT)
Significance	Other
Disease	p phenotype
Variation	info
Gene	A4GALT
CLNDBN	p phenotype
Reversed	1
HGVS	NC_000022.10:g.43089716_43089718delAAG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000002815.3,