Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.11 (C)

Chromosome 10:6010681 (forward strand) | View in location tab

Most severe consequence
Downstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 4 transcripts and has 2552 sample genotypes.

Variant displays