Original source

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

with HGMD-PUBLIC CS045643

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs60350369, rs3808334

This variant has 2 HGVS names - click the plus to show

7:g.155461298G>A
ENST00000297375.4:c.686-1073G>A

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