Original source

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

Alleles
AT/-
Location

Chromosome 19:10190804-10190805 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs142870756

This variant has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 1 sample genotype.

Variant displays