Original source

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

Alleles
-/TTC | MAF: 0.23 (TTC)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs147309883

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

Variation displays