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rs797045082

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045082(A;A)
Make rs797045082(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position49418978
GeneAMT
is asnp
is mentioned by
dbSNPrs797045082
ebirs797045082
HLIrs797045082
Exacrs797045082
Varsomers797045082
Maprs797045082
PheGenIrs797045082
hapmaprs797045082
1000 genomesrs797045082
hgdprs797045082
ensemblrs797045082
gopubmedrs797045082
geneviewrs797045082
scholarrs797045082
googlers797045082
pharmgkbrs797045082
gwascentralrs797045082
openSNPrs797045082
23andMers797045082
23andMe allrs797045082
SNP Nexus

SNPshotrs797045082
SNPdbers797045082
MSV3drs797045082
GWAS Ctlgrs797045082
Max Magnitude0
ClinVar
Risk rs797045082(A;A)
Alt rs797045082(A;A)
Reference rs797045082(G;G)
Significance Pathogenic
Disease Non-ketotic hyperglycinemia
Variation info
Gene AMT
CLNDBN Non-ketotic hyperglycinemia
Reversed 1
HGVS NC_000003.11:g.49456411C>T
CLNSRC
CLNACC RCV000190566.1,