Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.02 (C)

Chromosome 16:46675774 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs649672, rs252729

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 8 transcripts and has 3199 sample genotypes.

Variant displays