Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.39 (A)

Chromosome 10:124986120 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs3168030

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2581 sample genotypes.

Variant displays