Original source

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

T/- | Ancestral: T | MAF: 0.23 (-)

Chromosome 4:119152189 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2504 sample genotypes.

Variant displays