Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.23 (A)
Location

Chromosome 1:219913853 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2515 sample genotypes.

Variant displays