Original source

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

Alleles
-/GCGC
Location

Chromosome 7: between 38976624 and 38976625 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs141094777, rs67413322

HGVS name

7:g.38976624_38976625insGCGC

Variation displays