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rs376757912

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs376757912(A;A)
Make rs376757912(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position80280193
GeneMAT1A
is asnp
is mentioned by
dbSNPrs376757912
dbSNP (classic)rs376757912
ClinGenrs376757912
ebirs376757912
HLIrs376757912
Exacrs376757912
Gnomadrs376757912
Varsomers376757912
LitVarrs376757912
Maprs376757912
PheGenIrs376757912
Biobankrs376757912
1000 genomesrs376757912
hgdprs376757912
ensemblrs376757912
geneviewrs376757912
scholarrs376757912
googlers376757912
pharmgkbrs376757912
gwascentralrs376757912
openSNPrs376757912
23andMers376757912
23andMe allrs376757912
SNPshotrs376757912
SNPdbers376757912
MSV3drs376757912
GWAS Ctlgrs376757912
Max Magnitude0
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,