Original source

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

Alleles
-/A
Location

Chromosome 19: between 52188560 and 52188561 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.52188560_52188561insA

Variation displays