Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 1:113863923 (forward strand) | View in location tab

Co-located

with dbSNP rs369280519 (A/-)

Most severe consequence
 
Intron variant

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 1 sample genotype.

Variant displays