rs1057524499

Orientation

minus

Stabilized

minus

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

Make rs1057524499(A;T)

Make rs1057524499(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

1399005

Gene

GAMT

is a	snp
is	mentioned by
dbSNP	rs1057524499
dbSNP (classic)	rs1057524499
ClinGen	rs1057524499
ebi	rs1057524499
HLI	rs1057524499
Exac	rs1057524499
Gnomad	rs1057524499
Varsome	rs1057524499
LitVar	rs1057524499
Map	rs1057524499
PheGenI	rs1057524499
Biobank	rs1057524499
1000 genomes	rs1057524499
hgdp	rs1057524499
ensembl	rs1057524499
geneview	rs1057524499
scholar	rs1057524499
google	rs1057524499
pharmgkb	rs1057524499
gwascentral	rs1057524499
openSNP	rs1057524499
23andMe	rs1057524499
SNPshot	rs1057524499
SNPdbe	rs1057524499
MSV3d	rs1057524499
GWAS Ctlg	rs1057524499

Max Magnitude

0

ClinVar
Risk	rs1057524499(T;T)
Alt	rs1057524499(T;T)
Reference	Rs1057524499(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GAMT
CLNDBN	not provided
Reversed	1
HGVS	NC_000019.9:g.1399004T>A
CLNSRC
CLNACC	RCV000420204.1,