Original source

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

T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.49 (T)

Chromosome 14:104769221 (forward strand)|View in location tab

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs17846830, rs58330911

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 18 transcripts, 2 regulatory features, has 2595 sample genotypes and is mentioned in 2 citations.

Variant displays