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rs6129653

From SNPedia

Orientationplus
Make rs6129653(C;C)
Make rs6129653(C;T)
Make rs6129653(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position40646963
is asnp
is mentioned by
dbSNPrs6129653
ebirs6129653
HLIrs6129653
Exacrs6129653
Varsomers6129653
Maprs6129653
PheGenIrs6129653
hapmaprs6129653
1000 genomesrs6129653
hgdprs6129653
ensemblrs6129653
gopubmedrs6129653
geneviewrs6129653
scholarrs6129653
googlers6129653
pharmgkbrs6129653
gwascentralrs6129653
openSNPrs6129653
23andMers6129653
23andMe allrs6129653
SNP Nexus

SNPshotrs6129653
SNPdbers6129653
MSV3drs6129653
GWAS Ctlgrs6129653
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 27537108] Genetic variants of 20q12 contributed to non-syndromic orofacial clefts susceptibility.