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rs759157320

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs759157320(C;T)
Make rs759157320(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position75278290
GeneSLC25A19
is asnp
is mentioned by
dbSNPrs759157320
ebirs759157320
HLIrs759157320
Exacrs759157320
Varsomers759157320
Maprs759157320
PheGenIrs759157320
hapmaprs759157320
1000 genomesrs759157320
hgdprs759157320
ensemblrs759157320
gopubmedrs759157320
geneviewrs759157320
scholarrs759157320
googlers759157320
pharmgkbrs759157320
gwascentralrs759157320
openSNPrs759157320
23andMers759157320
23andMe allrs759157320
SNP Nexus

SNPshotrs759157320
SNPdbers759157320
MSV3drs759157320
GWAS Ctlgrs759157320
Max Magnitude0
ClinVar
Risk rs759157320(T;T)
Alt rs759157320(T;T)
Reference rs759157320(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC25A19
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.73274371C>T
CLNSRC
CLNACC RCV000171266.1,