Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.36 (C)
Location

Chromosome 14:74902643 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3199989, rs61044770

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and has 2627 sample genotypes.

Variant displays