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rs17734557

From SNPedia

Orientationplus
Stabilizedplus
Make rs17734557(C;C)
Make rs17734557(C;T)
Make rs17734557(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position51476359
is asnp
is mentioned by
dbSNPrs17734557
dbSNP (old)rs17734557
ClinGenrs17734557
ebirs17734557
HLIrs17734557
Exacrs17734557
Gnomadrs17734557
Varsomers17734557
Maprs17734557
PheGenIrs17734557
Biobankrs17734557
1000 genomesrs17734557
hgdprs17734557
ensemblrs17734557
gopubmedrs17734557
geneviewrs17734557
scholarrs17734557
googlers17734557
pharmgkbrs17734557
gwascentralrs17734557
openSNPrs17734557
23andMers17734557
23andMe allrs17734557
SNPshotrs17734557
SNPdbers17734557
MSV3drs17734557
GWAS Ctlgrs17734557
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.