Original source

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

Alleles
G/A/C|Ancestral: G|Ambiguity code: V|MAF: 0.01 (A)
Location

Chromosome 5:69277333 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and has 2504 sample genotypes.

Variant displays