Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.33 (A)

Chromosome 19:49933114 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs118042983

This variation has 10 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 68 transcripts, has 1349 individual genotypes and is mentioned in 2 citations.

Variation displays