Original source

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

A/C/G | Ancestral: G | Ambiguity code: V | MAF: 0.49 (G)

Chromosome 7:151150662 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, HumanOmniExpress, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 2841 sample genotypes.

Variant displays