Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 1:113847252 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57967793

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2 sample genotypes.

Variant displays