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 (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
-/C | Ancestral: G
Location

Chromosome 19:10135264 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs72572434

This variation has 18 HGVS names - click the plus to show

Variation displays