Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: < 0.01 (T)

Chromosome 6:43515485 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 28 transcripts and has 2504 sample genotypes.

Variant displays