Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: < 0.01 (A)
Location

Chromosome 7:151148563 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

7:g.151148563G>A

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts and has 2504 sample genotypes.

Variant displays