Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.02 (A)
Location

Chromosome 14:22501272 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

14:g.22501272C>A

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 7 transcripts and has 3628 sample genotypes.

Variant displays