Original source

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

Alleles
CT/-|MAF: 0.42 (-)
Location

Chromosome 4:41746722-41746723 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2508 sample genotypes.

Variant displays