Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 5:1266537 (forward strand) | View in location tab
with HGMD-PUBLIC CS072295
This variation has 16 HGVS names - click the plus to show
This variation has assays on: Illumina_HumanOmni5, Illumina_Human1M-duo
This variant overlaps 14 transcripts.