Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.15 (A)
Location

Chromosome 9:37429664 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

This variant has 2 synonyms - click the plus to show

This variant has 9 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 3765 sample genotypes.

Variant displays