Single nucleotide variant rs1011749

Genomic position: 16:

Allele info and frequencies

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This SNP has no significant association with diseases nor in high LD with index SNPs.


Click here to find this SNP in GTEx database.

There are no significant eQTL association in gene level to this SNP.

Transcript Level

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Transcript ID Discovered on cis/trans Distance p-value Regression coefficient eQTL plot More
ENST00000564047 Cerebellum cis-eQTL -63948 0.000000106632 -0.868474 Display eQTL plot

This SNP has no significant association with any pathology marker.