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rs542184779

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs542184779(A;A)
Make rs542184779(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position13110210
GeneTRMT1
is asnp
is mentioned by
dbSNPrs542184779
ebirs542184779
HLIrs542184779
Exacrs542184779
Varsomers542184779
Maprs542184779
PheGenIrs542184779
hapmaprs542184779
1000 genomesrs542184779
hgdprs542184779
ensemblrs542184779
gopubmedrs542184779
geneviewrs542184779
scholarrs542184779
googlers542184779
pharmgkbrs542184779
gwascentralrs542184779
openSNPrs542184779
23andMers542184779
23andMe allrs542184779
SNP Nexus

SNPshotrs542184779
SNPdbers542184779
MSV3drs542184779
GWAS Ctlgrs542184779
Max Magnitude0
ClinVar
Risk rs542184779(A;A)
Alt rs542184779(A;A)
Reference rs542184779(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TRMT1
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.13221024G>A
CLNSRC
CLNACC RCV000171278.1,