Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.30 (G)
Location

Chromosome 18:51074970 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2512 individual genotypes.

Variation displays