Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.06 (G)
Location

Chromosome 7:30969977 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

LSDB GHRHR_366+13T_G_041811

This variant has 6 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 10 transcripts, has 2505 sample genotypes and is associated with 1 phenotype.

Variant displays