Original source

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

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

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

Co-located

with HGMD-PUBLIC CR054251

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts and has 2537 individual genotypes.

Variation displays