Original source

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

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

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


with dbSNP rs112977316 (C/-)

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 7 transcripts and has 1100 individual genotypes.

Variation displays