Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.41 (T)

Chromosome 7:100823322 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs1647623

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts and has 2512 sample genotypes.

Variant displays