Original source

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

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

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

Co-located variant

dbSNP rs200688164 (A/T)

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2512 sample genotypes.

Variant displays