rs376757912

Orientation

plus

Stabilized

plus

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

Make rs376757912(A;A)

Make rs376757912(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

80280193

Gene

MAT1A

is a	snp
is	mentioned by
dbSNP	rs376757912
dbSNP (classic)	rs376757912
ClinGen	rs376757912
ebi	rs376757912
HLI	rs376757912
Exac	rs376757912
Gnomad	rs376757912
Varsome	rs376757912
LitVar	rs376757912
Map	rs376757912
PheGenI	rs376757912
Biobank	rs376757912
1000 genomes	rs376757912
hgdp	rs376757912
ensembl	rs376757912
geneview	rs376757912
scholar	rs376757912
google	rs376757912
pharmgkb	rs376757912
gwascentral	rs376757912
openSNP	rs376757912
23andMe	rs376757912
SNPshot	rs376757912
SNPdbe	rs376757912
MSV3d	rs376757912
GWAS Ctlg	rs376757912

Max Magnitude

0

ClinVar
Risk	rs376757912(A;A) rs376757912(T;T)
Alt	rs376757912(A;A) rs376757912(T;T)
Reference	Rs376757912(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MAT1A
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.82039949G>A
CLNSRC
CLNACC	RCV000489288.1,