Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.11 (T)

Chromosome 14:56800305 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs1681184, rs57897719

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2598 sample genotypes.

Variant displays