This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: < 0.01 (A)
Location

Chromosome 19:5831959 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

Variation displays