Original source

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

CT/- | MAF: 0.21 (-)

Chromosome 16:28882404-28882405 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs71856485, rs146965224

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 1093 individual genotypes.

Variation displays