Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.11 (G)
Location

Chromosome 11:6390089 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.6390089C>G

About this variant

This variant overlaps 11 transcripts and has 2537 individual genotypes.

Variation displays