Original source

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

A/G/T | Ancestral: A | Ambiguity code: D | MAF: 0.01 (G)

Chromosome 10:73997184 (forward strand) | View in location tab

Most severe consequence
Splice region variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 12 transcripts and has 2504 sample genotypes.

Variant displays