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

rs121908534

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908534(A;A)
Make rs121908534(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position40799213
GeneGPR82, SLC25A15
is asnp
is mentioned by
dbSNPrs121908534
ebirs121908534
HLIrs121908534
Exacrs121908534
Varsomers121908534
Maprs121908534
PheGenIrs121908534
hapmaprs121908534
1000 genomesrs121908534
hgdprs121908534
ensemblrs121908534
gopubmedrs121908534
geneviewrs121908534
scholarrs121908534
googlers121908534
pharmgkbrs121908534
gwascentralrs121908534
openSNPrs121908534
23andMers121908534
23andMe allrs121908534
SNP Nexus

SNPshotrs121908534
SNPdbers121908534
MSV3drs121908534
GWAS Ctlgrs121908534
Max Magnitude0
OMIM603861
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121908534(A;A)
Alt rs121908534(A;A)
Reference rs121908534(T;T)
Significance Pathogenic
Disease Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Variation info
Gene SLC25A15 TPTE2P5
CLNDBN Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Reversed 0
HGVS NC_000013.10:g.41373349T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006364.1,