Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/AAT | MAF: 0.39 (-)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs146838438

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2511 individual genotypes.

Variation displays