Original source

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

Alleles
-/AAAGC|MAF: 0.05 (AAAGC)
Location

Chromosome 2: between 236165404 and 236165405 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2504 sample genotypes.

Variant displays