Original source

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

Alleles
-/A
Location

Chromosome 7: between 101125474 and 101125475 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.101125474_101125475insA

Variation displays