Original source

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

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

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

Co-located variant

HGMD-PUBLIC CS014432

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60055022

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 13 transcripts and has 3801 sample genotypes.

Variant displays