rs1057523885

Orientation

plus

Stabilized

plus

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

Make rs1057523885(A;A)

Make rs1057523885(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

34647657

Gene

GALT

is a	snp
is	mentioned by
dbSNP	rs1057523885
dbSNP (classic)	rs1057523885
ClinGen	rs1057523885
ebi	rs1057523885
HLI	rs1057523885
Exac	rs1057523885
Gnomad	rs1057523885
Varsome	rs1057523885
LitVar	rs1057523885
Map	rs1057523885
PheGenI	rs1057523885
Biobank	rs1057523885
1000 genomes	rs1057523885
hgdp	rs1057523885
ensembl	rs1057523885
geneview	rs1057523885
scholar	rs1057523885
google	rs1057523885
pharmgkb	rs1057523885
gwascentral	rs1057523885
openSNP	rs1057523885
23andMe	rs1057523885
SNPshot	rs1057523885
SNPdbe	rs1057523885
MSV3d	rs1057523885
GWAS Ctlg	rs1057523885

Max Magnitude

0

ClinVar
Risk	rs1057523885(A;A)
Alt	rs1057523885(A;A)
Reference	Rs1057523885(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GALT
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.34647654G>A
CLNSRC
CLNACC	RCV000439035.1,