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rs1234747

From SNPedia

Orientationminus
Stabilizedminus
Make rs1234747(A;A)
Make rs1234747(A;G)
Make rs1234747(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position147795900
is asnp
is mentioned by
dbSNPrs1234747
ebirs1234747
HLIrs1234747
Exacrs1234747
Varsomers1234747
Maprs1234747
PheGenIrs1234747
hapmaprs1234747
1000 genomesrs1234747
hgdprs1234747
ensemblrs1234747
gopubmedrs1234747
geneviewrs1234747
scholarrs1234747
googlers1234747
pharmgkbrs1234747
gwascentralrs1234747
openSNPrs1234747
23andMers1234747
23andMe allrs1234747
SNP Nexus

SNPshotrs1234747
SNPdbers1234747
MSV3drs1234747
GWAS Ctlgrs1234747
Max Magnitude
nature The inheritance of the AC haplotype of rs1861972rs1861973, the C allele of rs1811399, and the C allele of rs1234747 may contribute to autism by affecting microRNA