Original source

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

Alleles
-/TG | MAF: 0.03 (TG)
Location

Chromosome 5: between 132869135 and 132869136 (forward strand) | View in location tab

Most severe consequence
HGVS name

5:g.132869135_132869136insTG

Variation displays