Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 15:90715523 (forward strand) | View in location tab
with dbSNP rs372755681 (G/-)
This variation has 4 HGVS names - click the plus to show
This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5
This variant overlaps 6 transcripts.