Original source

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

Alleles
T/-|Ancestral: T|MAF: 0.02 (-)
Location

Chromosome 2:236165254 (forward strand)|View in location tab

Co-located variant

dbSNP rs4292047 (T/C)

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs67252683

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2504 sample genotypes.

Variant displays