Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.18 (C)

Chromosome 1:12203760 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs9430685, rs17880016

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts and has 2552 sample genotypes.

Variant displays