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

rs796052527

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052527(A;G)
Make rs796052527(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position1401476
GeneGAMT
is asnp
is mentioned by
dbSNPrs796052527
ebirs796052527
HLIrs796052527
Exacrs796052527
Varsomers796052527
Maprs796052527
PheGenIrs796052527
hapmaprs796052527
1000 genomesrs796052527
hgdprs796052527
ensemblrs796052527
gopubmedrs796052527
geneviewrs796052527
scholarrs796052527
googlers796052527
pharmgkbrs796052527
gwascentralrs796052527
openSNPrs796052527
23andMers796052527
23andMe allrs796052527
SNP Nexus

SNPshotrs796052527
SNPdbers796052527
MSV3drs796052527
GWAS Ctlgrs796052527
Max Magnitude0
ClinVar
Risk rs796052527(G;G)
Alt rs796052527(G;G)
Reference rs796052527(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene GAMT
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.1401475T>C
CLNSRC
CLNACC RCV000187576.1,