Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.12 (T)
Location

Chromosome 7:155459499 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56973392

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 2776 sample genotypes and is mentioned in 5 citations.

Variant displays