Original source

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

-/TTC | MAF: 0.23 (TTC)

Chromosome 2: between 9489169 and 9489170 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs147309883

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts and has 1092 individual genotypes.

Variation displays