Single nucleotide variant rs10130660

Genomic position: 14:

Allele info and frequencies

Click here to go to dbSNP for more information.



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

Click on transcript id to go to that transcript. Cilck table header to sort by that attribute.

Transcript ID Discovered on cis/trans Distance p-value Regression coefficient eQTL plot More
ENST00000429687 Cerebellum cis-eQTL 3308 0.00000000604263 -1.08424 Display eQTL plot
ENST00000250416 Cerebellum cis-eQTL 3309 0.0000000019587 1.10898 Display eQTL plot
ENST00000527915 Cerebellum cis-eQTL 3310 0.0000000957558 1.01662 Display eQTL plot
ENST00000429687 Hippocampus cis-eQTL 3308 0.0000000000739942 -1.17318 Display eQTL plot
ENST00000250416 Hippocampus cis-eQTL 3309 0.0000000000180056 1.19777 Display eQTL plot
ENST00000250416 Orbitofrontal Cortex cis-eQTL 3309 0.00000000122387 1.11888 Display eQTL plot
ENST00000429687 Prefrontal Cortex cis-eQTL 3308 0.000000000118736 -1.17494 Display eQTL plot
ENST00000250416 Prefrontal Cortex cis-eQTL 3309 0.00000000000394191 1.2328 Display eQTL plot

This SNP has no significant association with any pathology marker.