Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.08 (C)
Location

Chromosome 14:104769487 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs61761252

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and has 2596 sample genotypes.

Variant displays