Original source

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

TTTG/- | MAF: 0.50 (-)

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