Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

-/C/G | MAF: 0.01 (G)

Chromosome 20: between 58652376 and 58652377 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 44 HGVS names - click the plus to show

About this variant

This variant overlaps 43 transcripts and has 1092 individual genotypes.

Variation displays