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rs7987165

From SNPedia

Orientationplus
Stabilizedplus
Make rs7987165(A;A)
Make rs7987165(A;C)
Make rs7987165(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position76570919
is asnp
is mentioned by
dbSNPrs7987165
ebirs7987165
HLIrs7987165
Exacrs7987165
Varsomers7987165
Maprs7987165
PheGenIrs7987165
hapmaprs7987165
1000 genomesrs7987165
hgdprs7987165
ensemblrs7987165
gopubmedrs7987165
geneviewrs7987165
scholarrs7987165
googlers7987165
pharmgkbrs7987165
gwascentralrs7987165
openSNPrs7987165
23andMers7987165
23andMe allrs7987165
SNP Nexus

SNPshotrs7987165
SNPdbers7987165
MSV3drs7987165
GWAS Ctlgrs7987165
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 25099202] Genetic risk factors for orofacial clefts in Central Africans and Southeast Asians