Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.17 (G)

Chromosome 14:103701601 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 22 transcripts and has 2601 sample genotypes.

Variant displays