Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/GCGC
Location

Chromosome 7: between 38976633 and 38976634 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

7:g.38976630_38976633dupGCGC

About this variant

This variant overlaps 1 transcript and has 9 individual genotypes.

Variation displays