Original source

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

Alleles
T/C|Ambiguity code: Y|MAF: 0.46 (C)
Location

Chromosome 16:28478025 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 27 HGVS names - Show

About this variant

This variant overlaps 34 transcripts and has 2510 sample genotypes.

Variant displays