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rs1316471

From SNPedia

Orientationplus
Stabilizedplus
Make rs1316471(C;C)
Make rs1316471(C;T)
Make rs1316471(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position51474384
is asnp
is mentioned by
dbSNPrs1316471
dbSNP (old)rs1316471
ClinGenrs1316471
ebirs1316471
HLIrs1316471
Exacrs1316471
Gnomadrs1316471
Varsomers1316471
Maprs1316471
PheGenIrs1316471
Biobankrs1316471
1000 genomesrs1316471
hgdprs1316471
ensemblrs1316471
gopubmedrs1316471
geneviewrs1316471
scholarrs1316471
googlers1316471
pharmgkbrs1316471
gwascentralrs1316471
openSNPrs1316471
23andMers1316471
23andMe allrs1316471
SNPshotrs1316471
SNPdbers1316471
MSV3drs1316471
GWAS Ctlgrs1316471
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 29535761OA-icon.png] A Genome-Wide Search for Gene-Environment Effects in Isolated Cleft Lip with or without Cleft Palate Triads Points to an Interaction between Maternal Periconceptional Vitamin Use and Variants in ESRRG.