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rs540026

From SNPedia

Merged intors183314
Orientationminus
Make rs540026(A;A)
Make rs540026(A;T)
Make rs540026(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position162176552
is asnp
is mentioned by
dbSNPrs540026
ebirs540026
HLIrs540026
Exacrs540026
Varsomers540026
Maprs540026
PheGenIrs540026
hapmaprs540026
1000 genomesrs540026
hgdprs540026
ensemblrs540026
gopubmedrs540026
geneviewrs540026
scholarrs540026
googlers540026
pharmgkbrs540026
gwascentralrs540026
openSNPrs540026
23andMers540026
23andMe allrs540026
SNP Nexus

SNPshotrs540026
SNPdbers540026
MSV3drs540026
GWAS Ctlgrs540026
StatusMerged into rs183314
Max Magnitude

[PMID 26586245] Polymorphic variants near 1p22 and 20q11.2 loci and the risk of non-syndromic cleft lip and palate in South Indian population