Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2512 sample genotypes.

Variant displays