Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 11:1994893 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.1994893G>A

About this variant

This variant overlaps 19 transcripts and has 2504 individual genotypes.

Variation displays