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rs199894905

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199894905(G;T)
Make rs199894905(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position40805140
GeneGPR82, SLC25A15
is asnp
is mentioned by
dbSNPrs199894905
ebirs199894905
HLIrs199894905
Exacrs199894905
Varsomers199894905
Maprs199894905
PheGenIrs199894905
hapmaprs199894905
1000 genomesrs199894905
hgdprs199894905
ensemblrs199894905
gopubmedrs199894905
geneviewrs199894905
scholarrs199894905
googlers199894905
pharmgkbrs199894905
gwascentralrs199894905
openSNPrs199894905
23andMers199894905
23andMe allrs199894905
SNP Nexus

SNPshotrs199894905
SNPdbers199894905
MSV3drs199894905
GWAS Ctlgrs199894905
Max Magnitude0
ClinVar
Risk rs199894905(A,T;A,T)
Alt rs199894905(A,T;A,T)
Reference rs199894905(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.41379276G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000031949.1,