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rs753198836

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs753198836(A;A)
Make rs753198836(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position1399587
GeneGAMT
is asnp
is mentioned by
dbSNPrs753198836
ebirs753198836
HLIrs753198836
Exacrs753198836
Varsomers753198836
Maprs753198836
PheGenIrs753198836
hapmaprs753198836
1000 genomesrs753198836
hgdprs753198836
ensemblrs753198836
gopubmedrs753198836
geneviewrs753198836
scholarrs753198836
googlers753198836
pharmgkbrs753198836
gwascentralrs753198836
openSNPrs753198836
23andMers753198836
23andMe allrs753198836
SNP Nexus

SNPshotrs753198836
SNPdbers753198836
MSV3drs753198836
GWAS Ctlgrs753198836
Max Magnitude0
ClinVar
Risk rs753198836(A;A)
Alt rs753198836(A;A)
Reference rs753198836(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GAMT
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.1399586C>A
CLNSRC
CLNACC RCV000187565.2,