Original source

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

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

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

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

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