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rs17208928

From SNPedia

Orientationplus
Make rs17208928(C;C)
Make rs17208928(C;T)
Make rs17208928(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position122627023
GenePARP15
is asnp
is mentioned by
dbSNPrs17208928
ebirs17208928
HLIrs17208928
Exacrs17208928
Varsomers17208928
Maprs17208928
PheGenIrs17208928
hapmaprs17208928
1000 genomesrs17208928
hgdprs17208928
ensemblrs17208928
gopubmedrs17208928
geneviewrs17208928
scholarrs17208928
googlers17208928
pharmgkbrs17208928
gwascentralrs17208928
openSNPrs17208928
23andMers17208928
23andMe allrs17208928
SNP Nexus

SNPshotrs17208928
SNPdbers17208928
MSV3drs17208928
GWAS Ctlgrs17208928
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 27610459] Genetic Association of PARP15 Polymorphisms with Clinical Outcome of Acute Myeloid Leukemia in a Korean Population.