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rs2747022

From SNPedia

Orientationplus
Stabilizedplus
Make rs2747022(C;C)
Make rs2747022(C;T)
Make rs2747022(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position132126844
GeneFRMD7
is asnp
is mentioned by
dbSNPrs2747022
ebirs2747022
HLIrs2747022
Exacrs2747022
Varsomers2747022
Maprs2747022
PheGenIrs2747022
hapmaprs2747022
1000 genomesrs2747022
hgdprs2747022
ensemblrs2747022
gopubmedrs2747022
geneviewrs2747022
scholarrs2747022
googlers2747022
pharmgkbrs2747022
gwascentralrs2747022
openSNPrs2747022
23andMers2747022
23andMe allrs2747022
SNP Nexus

SNPshotrs2747022
SNPdbers2747022
MSV3drs2747022
GWAS Ctlgrs2747022
GMAF0.3513
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23613933OA-icon.png] X-Chromosomal Maternal and Fetal SNPs and the Risk of Spontaneous Preterm Delivery in a Danish/Norwegian Genome-Wide Association Study