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: 0.23 (C)
Location

Chromosome 19:40749595 (forward strand) | View in location tab

Co-located

with COSMIC COSM3823143 (C/G)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58684549, rs17608836

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 19 transcripts and has 1434 individual genotypes.

Variation displays