Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.33 (C)

Chromosome 6:10402950 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 16 transcripts, has 3876 sample genotypes and is mentioned in 2 citations.

Variant displays