Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 22:23314599 (forward strand) | View in location tab
with COSMIC COSM3785508 (C/G)
This variation has 8 HGVS names - click the plus to show
This variation has assays on: Illumina_ExomeChip
This variant overlaps 8 transcripts.