Original source

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

Alleles
-/A | MAF: 0.01 (-)
Location

Chromosome 19: between 42338967 and 42338968 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs144082434

This variation has 4 HGVS names - click the plus to show

Variation displays