Original source

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

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