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rs759454598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs759454598(G;T)
Make rs759454598(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position40799092
GeneSLC25A15, TPTE2P5
is asnp
is mentioned by
dbSNPrs759454598
dbSNP (classic)rs759454598
ClinGenrs759454598
ebirs759454598
HLIrs759454598
Exacrs759454598
Gnomadrs759454598
Varsomers759454598
LitVarrs759454598
Maprs759454598
PheGenIrs759454598
Biobankrs759454598
1000 genomesrs759454598
hgdprs759454598
ensemblrs759454598
geneviewrs759454598
scholarrs759454598
googlers759454598
pharmgkbrs759454598
gwascentralrs759454598
openSNPrs759454598
23andMers759454598
SNPshotrs759454598
SNPdbers759454598
MSV3drs759454598
GWAS Ctlgrs759454598
Max Magnitude0
ClinVar
Risk rs759454598(A;A) rs759454598(C;C) rs759454598(T;T)
Alt rs759454598(A;A) rs759454598(C;C) rs759454598(T;T)
Reference Rs759454598(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC25A15 TPTE2P5
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.41373228G>C
CLNSRC
CLNACC RCV000484190.1,