Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.29 (G)

Chromosome 5:69254808 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs3816867

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 15 transcripts and has 2841 sample genotypes.

Variant displays