Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.22 (G)
Location

Chromosome 19:33390741 (forward strand) | View in location tab

Co-located

with dbSNP rs112977316 (C/-)

Most severe consequence
Evidence status

This variation has 5 HGVS names - click the plus to show

Variation displays