Original source

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

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

Chromosome 4: between 110474913 and 110474914 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2504 sample genotypes.

Variant displays