Original source

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

Alleles
-/C | MAF: 0.25 (-)
Location

Chromosome 18: between 5437962 and 5437963 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2517 individual genotypes.

Variation displays