rs370421531

Orientation

plus

Stabilized

plus

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

Make rs370421531(C;T)

Make rs370421531(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

19

Position

1398964

Gene

GAMT

is a	snp
is	mentioned by
dbSNP	rs370421531
dbSNP (classic)	rs370421531
ClinGen	rs370421531
ebi	rs370421531
HLI	rs370421531
Exac	rs370421531
Gnomad	rs370421531
Varsome	rs370421531
LitVar	rs370421531
Map	rs370421531
PheGenI	rs370421531
Biobank	rs370421531
1000 genomes	rs370421531
hgdp	rs370421531
ensembl	rs370421531
geneview	rs370421531
scholar	rs370421531
google	rs370421531
pharmgkb	rs370421531
gwascentral	rs370421531
openSNP	rs370421531
23andMe	rs370421531
SNPshot	rs370421531
SNPdbe	rs370421531
MSV3d	rs370421531
GWAS Ctlg	rs370421531

Max Magnitude

0

ClinVar
Risk	rs370421531(T;T)
Alt	rs370421531(T;T)
Reference	Rs370421531(C;C)
Significance	Pathogenic
Disease	not provided Deficiency of guanidinoacetate methyltransferase
Variation	info
Gene	GAMT
CLNDBN	not provided Deficiency of guanidinoacetate methyltransferase
Reversed	0
HGVS	NC_000019.9:g.1398963C>T
CLNSRC
CLNACC	RCV000187569.1, RCV000316896.1,