This variation has been flagged

None of the variant alleles match the reference allele (G)

Original source

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

Alleles
-/T | Ancestral: G
Location

Chromosome 22:23521470 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.23521470G>T

Variation displays