Original source

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

-/C | MAF: 0.46 (C)

Chromosome 12: between 52794425 and 52794426 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2509 sample genotypes.

Variant displays