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rs12187557

From SNPedia

Orientationplus
Stabilizedplus
Make rs12187557(C;C)
Make rs12187557(C;T)
Make rs12187557(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position8439557
GeneSNORD19B
is asnp
is mentioned by
dbSNPrs12187557
ebirs12187557
HLIrs12187557
Exacrs12187557
Varsomers12187557
Maprs12187557
PheGenIrs12187557
hapmaprs12187557
1000 genomesrs12187557
hgdprs12187557
ensemblrs12187557
gopubmedrs12187557
geneviewrs12187557
scholarrs12187557
googlers12187557
pharmgkbrs12187557
gwascentralrs12187557
openSNPrs12187557
23andMers12187557
23andMe allrs12187557
SNP Nexus

SNPshotrs12187557
SNPdbers12187557
MSV3drs12187557
GWAS Ctlgrs12187557
GMAF0.314
Max Magnitude
? (C;C) (C;T) (T;T) 28


GET Evidence
rs12187557
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.640625
summary