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rs376993881

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs376993881(A;A)
Make rs376993881(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position80275073
GeneMAT1A
is asnp
is mentioned by
dbSNPrs376993881
dbSNP (classic)rs376993881
ClinGenrs376993881
ebirs376993881
HLIrs376993881
Exacrs376993881
Gnomadrs376993881
Varsomers376993881
LitVarrs376993881
Maprs376993881
PheGenIrs376993881
Biobankrs376993881
1000 genomesrs376993881
hgdprs376993881
ensemblrs376993881
geneviewrs376993881
scholarrs376993881
googlers376993881
pharmgkbrs376993881
gwascentralrs376993881
openSNPrs376993881
23andMers376993881
23andMe allrs376993881
SNPshotrs376993881
SNPdbers376993881
MSV3drs376993881
GWAS Ctlgrs376993881
Max Magnitude0
ClinVar
Risk rs376993881(A;A)
Alt rs376993881(A;A)
Reference Rs376993881(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MAT1A
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.82034829G>A
CLNSRC
CLNACC RCV000481494.1,