Original source

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

A/T | Ancestral: T | Ambiguity code: W | MAF: 0.35 (A)

Chromosome 5:132299399 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs36128629

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2507 individual genotypes.

Variation displays