Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ambiguity code: Y | MAF: 0.22 (C)
Location

Chromosome 14:21633418 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

14:g.21633418C>T

About this variant

This variant overlaps 1 transcript and has 2505 sample genotypes.

Variant displays