Original source

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

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

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