Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 1:201359243 (forward strand) | View in location tab
with COSMIC COSM209474 (G/A)
This variation has 14 HGVS names - click the plus to show
This variation has assays on: Illumina_HumanOmni1-Quad
This variant overlaps 19 transcripts.