Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.32 (T)

Chromosome 18:6941663 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs61692496

HGVS name


Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 5 transcripts, has 3972 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays