rs760101382

Orientation

plus

Stabilized

plus

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

Make rs760101382(C;T)

Make rs760101382(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

19

Position

1398995

Gene

GAMT

is a	snp
is	mentioned by
dbSNP	rs760101382
dbSNP (classic)	rs760101382
ClinGen	rs760101382
ebi	rs760101382
HLI	rs760101382
Exac	rs760101382
Gnomad	rs760101382
Varsome	rs760101382
LitVar	rs760101382
Map	rs760101382
PheGenI	rs760101382
Biobank	rs760101382
1000 genomes	rs760101382
hgdp	rs760101382
ensembl	rs760101382
geneview	rs760101382
scholar	rs760101382
google	rs760101382
pharmgkb	rs760101382
gwascentral	rs760101382
openSNP	rs760101382
23andMe	rs760101382
SNPshot	rs760101382
SNPdbe	rs760101382
MSV3d	rs760101382
GWAS Ctlg	rs760101382

Max Magnitude

0

ClinVar
Risk	rs760101382(T;T)
Alt	rs760101382(T;T)
Reference	Rs760101382(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GAMT
CLNDBN	not provided
Reversed	0
HGVS	NC_000019.9:g.1398994C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000187566.1,