Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y
Location

Chromosome 2:85657881 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 6 transcripts.

Variant displays