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rs17628931

From SNPedia

Orientationplus
Stabilizedplus
Make rs17628931(C;C)
Make rs17628931(C;T)
Make rs17628931(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position170109656
is asnp
is mentioned by
dbSNPrs17628931
ebirs17628931
HLIrs17628931
Exacrs17628931
Varsomers17628931
Maprs17628931
PheGenIrs17628931
hapmaprs17628931
1000 genomesrs17628931
hgdprs17628931
ensemblrs17628931
gopubmedrs17628931
geneviewrs17628931
scholarrs17628931
googlers17628931
pharmgkbrs17628931
gwascentralrs17628931
openSNPrs17628931
23andMers17628931
23andMe allrs17628931
SNP Nexus

SNPshotrs17628931
SNPdbers17628931
MSV3drs17628931
GWAS Ctlgrs17628931
GMAF0.04316
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23828458OA-icon.png] Identification of two maternal transmission ratio distortion loci in pedigrees of the Framingham heart study.