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]

-/C | Ancestral: G

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

Most severe consequence
Evidence status


Archive dbSNP rs72572434

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

About this variant

This variant overlaps 24 transcripts.

Variation displays