rs104893683

Orientation

minus

Stabilized

minus

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

Make rs104893683(A;A)

Make rs104893683(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

161085944

Gene

B3GALNT1

is a	snp
is	mentioned by
dbSNP	rs104893683
dbSNP (classic)	rs104893683
ClinGen	rs104893683
ebi	rs104893683
HLI	rs104893683
Exac	rs104893683
Gnomad	rs104893683
Varsome	rs104893683
LitVar	rs104893683
Map	rs104893683
PheGenI	rs104893683
Biobank	rs104893683
1000 genomes	rs104893683
hgdp	rs104893683
ensembl	rs104893683
geneview	rs104893683
scholar	rs104893683
google	rs104893683
pharmgkb	rs104893683
gwascentral	rs104893683
openSNP	rs104893683
23andMe	rs104893683
SNPshot	rs104893683
SNPdbe	rs104893683
MSV3d	rs104893683
GWAS Ctlg	rs104893683

Max Magnitude

0

OMIM	603094
Desc
Variant	0003
Related	also

ClinVar
Risk	rs104893683(A;A) rs104893683(T;T)
Alt	rs104893683(A;A) rs104893683(T;T)
Reference	Rs104893683(G;G)
Significance	Other
Disease	p phenotype
Variation	info
Gene	B3GALNT1
CLNDBN	p phenotype
Reversed	1
HGVS	NC_000003.11:g.160803732C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007014.3,