Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.04 (G)

Chromosome 6:154076193 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 18 transcripts, has 2788 sample genotypes and is mentioned in 1 citation.

Variant displays