Original source

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

-/A | MAF: 0.30 (A)

Chromosome 4: between 120697801 and 120697802 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2512 sample genotypes.

Variant displays