Original source

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

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.05 (G)

Chromosome 16:88646805 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs58454752, rs4987131

HGVS names

This variant has 19 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

About this variant

This variant overlaps 11 transcripts and has 3677 sample genotypes.

Variant displays