Original source

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

Alleles
-/A
Location

Chromosome 7: between 100768755 and 100768756 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.100768755_100768756insA

Variation displays