rs796052525

Orientation

minus

Stabilized

minus

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

Make rs796052525(G;T)

Make rs796052525(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

19

Position

1398960

Gene

GAMT

is a	snp
is	mentioned by
dbSNP	rs796052525
dbSNP (classic)	rs796052525
ClinGen	rs796052525
ebi	rs796052525
HLI	rs796052525
Exac	rs796052525
Gnomad	rs796052525
Varsome	rs796052525
LitVar	rs796052525
Map	rs796052525
PheGenI	rs796052525
Biobank	rs796052525
1000 genomes	rs796052525
hgdp	rs796052525
ensembl	rs796052525
geneview	rs796052525
scholar	rs796052525
google	rs796052525
pharmgkb	rs796052525
gwascentral	rs796052525
openSNP	rs796052525
23andMe	rs796052525
SNPshot	rs796052525
SNPdbe	rs796052525
MSV3d	rs796052525
GWAS Ctlg	rs796052525

Max Magnitude

0

ClinVar
Risk	rs796052525(T;T)
Alt	rs796052525(T;T)
Reference	Rs796052525(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GAMT
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.1398959C>A
CLNSRC
CLNACC	RCV000187571.1,