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rs202247804

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202247804(A;A)
Make rs202247804(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position40807410
GeneGPR82, SLC25A15
is asnp
is mentioned by
dbSNPrs202247804
ebirs202247804
HLIrs202247804
Exacrs202247804
Varsomers202247804
Maprs202247804
PheGenIrs202247804
hapmaprs202247804
1000 genomesrs202247804
hgdprs202247804
ensemblrs202247804
gopubmedrs202247804
geneviewrs202247804
scholarrs202247804
googlers202247804
pharmgkbrs202247804
gwascentralrs202247804
openSNPrs202247804
23andMers202247804
23andMe allrs202247804
SNP Nexus

SNPshotrs202247804
SNPdbers202247804
MSV3drs202247804
GWAS Ctlgrs202247804
Max Magnitude0
ClinVar
Risk rs202247804(A;A)
Alt rs202247804(A;A)
Reference rs202247804(G;G)
Significance Pathogenic
Disease Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Variation info
Gene SLC25A15 TPTE2P5
CLNDBN Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
Reversed 0
HGVS NC_000013.10:g.41381546G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000031952.1,