Original source

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

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

Chromosome 19:48987362 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_037958

This variation has 9 HGVS names - click the plus to show

Variation displays