Original source

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

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

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

Co-located variant

dbSNP rs369280519 (A/-)

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 1 sample genotype.

Variant displays