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rs12381366

From SNPedia

Merged intors9639947
Orientationplus
Make rs12381366(A;A)
Make rs12381366(A;G)
Make rs12381366(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome7
Position46237900
GeneLOC107986792
is asnp
is mentioned by
dbSNPrs12381366
dbSNP (classic)rs12381366
ClinGenrs12381366
ebirs12381366
HLIrs12381366
Exacrs12381366
Gnomadrs12381366
Varsomers12381366
LitVarrs12381366
Maprs12381366
PheGenIrs12381366
Biobankrs12381366
1000 genomesrs12381366
hgdprs12381366
ensemblrs12381366
geneviewrs12381366
scholarrs12381366
googlers12381366
pharmgkbrs12381366
gwascentralrs12381366
openSNPrs12381366
23andMers12381366
SNPshotrs12381366
SNPdbers12381366
MSV3drs12381366
GWAS Ctlgrs12381366
StatusMerged into rs9639947
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 30172247] Association between PTCH1 and RAD54B single-nucleotide polymorphisms and non-syndromic orofacial clefts in a northern Chinese population.