Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.37 (T)

Chromosome 3:184373361 (forward strand) | View in location tab


with HGMD-PUBLIC CS014432

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60055022

This variant has 6 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 2663 sample genotypes.

Variant displays