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

rs104894424

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894424(A;A)
Make rs104894424(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position40807379
GeneGPR82, SLC25A15
is asnp
is mentioned by
dbSNPrs104894424
ebirs104894424
HLIrs104894424
Exacrs104894424
Varsomers104894424
Maprs104894424
PheGenIrs104894424
hapmaprs104894424
1000 genomesrs104894424
hgdprs104894424
ensemblrs104894424
gopubmedrs104894424
geneviewrs104894424
scholarrs104894424
googlers104894424
pharmgkbrs104894424
gwascentralrs104894424
openSNPrs104894424
23andMers104894424
23andMe allrs104894424
SNP Nexus

SNPshotrs104894424
SNPdbers104894424
MSV3drs104894424
GWAS Ctlgrs104894424
Max Magnitude0
OMIM603861
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894424(A;A)
Alt rs104894424(A;A)
Reference rs104894424(G;G)
Significance Pathogenic
Disease Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome not provided
Variation info
Gene SLC25A15 TPTE2P5
CLNDBN Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome not provided
Reversed 0
HGVS NC_000013.10:g.41381515G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006359.1, RCV000186164.1,