Original source

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

Alleles
TTTG/-|MAF: 0.50 (-)
Location

Chromosome 18:5422460-5422463 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and has 2510 sample genotypes.

Variant displays