Original source

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

TTTG/- | MAF: 0.46 (TTTG)

Chromosome 18:5422460-5422463 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 1098 individual genotypes.

Variation displays