rs796051968

Orientation

plus

Stabilized

plus

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

Make rs796051968(A;A)

Make rs796051968(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

34649413

Gene

GALT

is a	snp
is	mentioned by
dbSNP	rs796051968
dbSNP (classic)	rs796051968
ClinGen	rs796051968
ebi	rs796051968
HLI	rs796051968
Exac	rs796051968
Gnomad	rs796051968
Varsome	rs796051968
LitVar	rs796051968
Map	rs796051968
PheGenI	rs796051968
Biobank	rs796051968
1000 genomes	rs796051968
hgdp	rs796051968
ensembl	rs796051968
geneview	rs796051968
scholar	rs796051968
google	rs796051968
pharmgkb	rs796051968
gwascentral	rs796051968
openSNP	rs796051968
23andMe	rs796051968
SNPshot	rs796051968
SNPdbe	rs796051968
MSV3d	rs796051968
GWAS Ctlg	rs796051968

Max Magnitude

0

ClinVar
Risk	rs796051968(A;A)
Alt	rs796051968(A;A)
Reference	Rs796051968(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GALT
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.34649410C>A
CLNSRC
CLNACC	RCV000185921.1,