Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: < 0.01 (C)

Chromosome 5:161847800 (forward strand) | View in location tab


with HGMD-PUBLIC CR054251

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts and has 2760 sample genotypes.

Variant displays