Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 4:73742161 (forward strand) | View in location tab
with dbSNP rs375781159 (A/-)
This variation has 3 HGVS names - click the plus to show
This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5
This variant overlaps 4 transcripts.