Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.21 (C)
Location

Chromosome 14:19919519 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

14:g.19919519T>C

About this variant

This variant overlaps 1 transcript and has 2509 sample genotypes.

Variant displays