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rs760101382

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs760101382(C;T)
Make rs760101382(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position1398995
GeneGAMT
is asnp
is mentioned by
dbSNPrs760101382
ebirs760101382
HLIrs760101382
Exacrs760101382
Varsomers760101382
Maprs760101382
PheGenIrs760101382
hapmaprs760101382
1000 genomesrs760101382
hgdprs760101382
ensemblrs760101382
gopubmedrs760101382
geneviewrs760101382
scholarrs760101382
googlers760101382
pharmgkbrs760101382
gwascentralrs760101382
openSNPrs760101382
23andMers760101382
23andMe allrs760101382
SNP Nexus

SNPshotrs760101382
SNPdbers760101382
MSV3drs760101382
GWAS Ctlgrs760101382
Max Magnitude0
ClinVar
Risk rs760101382(T;T)
Alt rs760101382(T;T)
Reference rs760101382(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GAMT
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.1398994C>T
CLNSRC
CLNACC RCV000187566.1,