Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.24 (G)
Location

Chromosome 7:155461298 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CS045643

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs60350369, rs3808334

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 2511 sample genotypes, is associated with 2 phenotypes and is mentioned in 16 citations.

Variant displays