Original source

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

T/G | Ancestral: T | Ambiguity code: K | MAF: 0.28 (T)

Chromosome 6:166157676 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status


Archive dbSNP rs3816306, rs60732233

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, has 2774 sample genotypes and is mentioned in 1 citation.

Variant displays