Original source

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

-/T | MAF: 0.48 (T)

Chromosome 2: between 231512722 and 231512723 (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 2511 sample genotypes.

Variant displays