Original source

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

Alleles
-/TGTGTGTGTGTGTGTG/TGTGT/TGTGTGTGTGTGT/TGT
Location

Chromosome 12: between 117208422 and 117208423 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 12 HGVS names - click the plus to show

Variation displays