Original source

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

Alleles
-/A | MAF: < 0.01 (-)
Location

Chromosome 19: between 42338967 and 42338968 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs144082434

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2513 sample genotypes.

Variant displays