Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.01 (C)

Chromosome 2:112830624 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs11567877

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 8 transcripts and has 2620 sample genotypes.

Variant displays