Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052525

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052525(G;T)
Make rs796052525(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position1398960
GeneGAMT
is asnp
is mentioned by
dbSNPrs796052525
ebirs796052525
HLIrs796052525
Exacrs796052525
Varsomers796052525
Maprs796052525
PheGenIrs796052525
hapmaprs796052525
1000 genomesrs796052525
hgdprs796052525
ensemblrs796052525
gopubmedrs796052525
geneviewrs796052525
scholarrs796052525
googlers796052525
pharmgkbrs796052525
gwascentralrs796052525
openSNPrs796052525
23andMers796052525
23andMe allrs796052525
SNP Nexus

SNPshotrs796052525
SNPdbers796052525
MSV3drs796052525
GWAS Ctlgrs796052525
Max Magnitude0
ClinVar
Risk rs796052525(T;T)
Alt rs796052525(T;T)
Reference rs796052525(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GAMT
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.1398959C>A
CLNSRC
CLNACC RCV000187571.1,