Original source

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

Alleles
A/- | Ancestral: A | MAF: 0.12 (A)
Location

Chromosome 14:56800284 (forward strand) | View in location tab

Co-located

with dbSNP rs200688164 (A/T)

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2512 sample genotypes.

Variant displays