Original source

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

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2513 sample genotypes.

Variant displays