rs796052527

Orientation

minus

Stabilized

minus

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

Make rs796052527(A;G)

Make rs796052527(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

19

Position

1401476

Gene

GAMT

is a	snp
is	mentioned by
dbSNP	rs796052527
dbSNP (classic)	rs796052527
ClinGen	rs796052527
ebi	rs796052527
HLI	rs796052527
Exac	rs796052527
Gnomad	rs796052527
Varsome	rs796052527
LitVar	rs796052527
Map	rs796052527
PheGenI	rs796052527
Biobank	rs796052527
1000 genomes	rs796052527
hgdp	rs796052527
ensembl	rs796052527
geneview	rs796052527
scholar	rs796052527
google	rs796052527
pharmgkb	rs796052527
gwascentral	rs796052527
openSNP	rs796052527
23andMe	rs796052527
SNPshot	rs796052527
SNPdbe	rs796052527
MSV3d	rs796052527
GWAS Ctlg	rs796052527

Max Magnitude

0

ClinVar
Risk	rs796052527(G;G)
Alt	rs796052527(G;G)
Reference	Rs796052527(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GAMT
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.1401475T>C
CLNSRC
CLNACC	RCV000187576.1,