Original source

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

TG/- | MAF: 0.31 (-)

Chromosome 8:42482737-42482738 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs143885739

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 1094 individual genotypes.

Variation displays