Original source

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

Alleles
-/A
Location

Chromosome 10: between 102242928 and 102242929 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

10:g.102242928_102242929insA

Variation displays