Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.02 (T)
Location

Chromosome 2:112830260 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2575 sample genotypes.

Variant displays