Original source

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

Alleles
AT/-
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs142870756

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 1 sample genotype.

Variant displays