Original source

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

Alleles
CCTGGGGGGTCTTCTAACTACTGG/- | MAF: 0.39 (-)
Location

Chromosome 1:109603137-109603160 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2512 sample genotypes.

Variant displays