Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.15 (C)

Chromosome 14:77275860 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs59818538

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2509 sample genotypes.

Variant displays