Original source

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

Alleles
-/G
Location

Chromosome 7: between 101126425 and 101126426 (forward strand) | View in location tab

Co-located

with dbSNP rs1799768 (-/G)

Most severe consequence
Evidence status

HGVS name

7:g.101126425_101126426insG

About this variant

This variant overlaps 4 transcripts, has 1141 individual genotypes and is mentioned in 5 citations.

Variation displays