Original source

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

-/TTG | MAF: 0.03 (TTG)

Chromosome 2: between 9489156 and 9489157 (forward strand) | View in location tab

Most severe consequence

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