Original source

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

-/AAT | MAF: 0.39 (-)

Chromosome 5: between 162071011 and 162071012 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs146838438

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2511 sample genotypes.

Variant displays