Original source

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

Alleles
G/A|Ambiguity code: R
Location

Chromosome 1:120840594 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 267 sample genotypes.

Variant displays