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rs1369766

From SNPedia

Orientationminus
Stabilizedminus
Make rs1369766(A;A)
Make rs1369766(A;G)
Make rs1369766(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position51492510
GeneRPS26P43
is asnp
is mentioned by
dbSNPrs1369766
ebirs1369766
HLIrs1369766
Exacrs1369766
Varsomers1369766
Maprs1369766
PheGenIrs1369766
hapmaprs1369766
1000 genomesrs1369766
hgdprs1369766
ensemblrs1369766
gopubmedrs1369766
geneviewrs1369766
scholarrs1369766
googlers1369766
pharmgkbrs1369766
gwascentralrs1369766
openSNPrs1369766
23andMers1369766
23andMe allrs1369766
SNP Nexus

SNPshotrs1369766
SNPdbers1369766
MSV3drs1369766
GWAS Ctlgrs1369766
GMAF0.4426
Max Magnitude
? (A;A) (A;G) (G;G) 28
OMIM251850
DescDIARRHEA 2, WITH MICROVILLOUS ATROPHY; DIAR2
Variant
Relatedalso
[PMID 17564975OA-icon.png] Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.