Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.05 (C)
Location

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

Co-located variant

dbSNP rs67252682 (T/-)

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 5 transcripts and has 3181 sample genotypes.

Variant displays