Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.34 (C)

Chromosome 16:67979568 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs1082687, rs59804968

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 12 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3522 sample genotypes, is associated with 3 phenotypes and is mentioned in 2 citations.

Variant displays