Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.02 (T)

Chromosome 4:127921414 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2504 sample genotypes.

Variant displays