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rs17807815

From SNPedia

Orientationplus
Stabilizedplus
Make rs17807815(C;C)
Make rs17807815(C;T)
Make rs17807815(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position92089711
GeneATXN3
is asnp
is mentioned by
dbSNPrs17807815
dbSNP (classic)rs17807815
ClinGenrs17807815
ebirs17807815
HLIrs17807815
Exacrs17807815
Gnomadrs17807815
Varsomers17807815
LitVarrs17807815
Maprs17807815
PheGenIrs17807815
Biobankrs17807815
1000 genomesrs17807815
hgdprs17807815
ensemblrs17807815
geneviewrs17807815
scholarrs17807815
googlers17807815
pharmgkbrs17807815
gwascentralrs17807815
openSNPrs17807815
23andMers17807815
SNPshotrs17807815
SNPdbers17807815
MSV3drs17807815
GWAS Ctlgrs17807815
GMAF0.07208
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22419666OA-icon.png]
Trait
Title Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.
Risk Allele
P-val 0.000006
Odds Ratio 2.3800 None