Original source

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

Alleles
A/G | Ambiguity code: R | MAF: 0.45 (A)
Location

Chromosome 11:18264546 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.18264546A>G

About this variant

This variant overlaps 5 transcripts and has 2508 individual genotypes.

Variation displays