Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.08 (A)

Chromosome 4:95449084 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59947849

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 4 transcripts and has 3694 sample genotypes.

Variant displays