Original source

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

Alleles
-/C | MAF: 0.34 (-)
Location

Chromosome 7: between 100718925 and 100718926 (forward strand) | View in location tab

Most severe consequence
HGVS name

7:g.100718925_100718926insC

About this variant

This variant overlaps 1 transcript and has 1092 individual genotypes.

Variation displays