Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.30 (T)
Location

Chromosome 14:22860237 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms
HGVS name

14:g.22860237T>C

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant has 3961 sample genotypes.

Variant displays