Original source

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

Alleles
-/T/TT/TTT|MAF: 0.18 (T)
Location

Chromosome 4: between 174519218 and 174519219 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 39 HGVS names - Show

About this variant

This variant overlaps 39 transcripts and has 2505 sample genotypes.

Variant displays