Original source

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

Alleles
-/G | MAF: 0.23 (-)
Location

Chromosome 19: between 16485848 and 16485849 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs376552064

This variation has 6 HGVS names - click the plus to show

Variation displays