Original source

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

Alleles
-/GCGC
Location

Chromosome 7: between 39016223 and 39016224 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.39016223_39016224insGCGC

Variation displays