Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 5:254484 (forward strand) | View in location tab
This variation has 3 synonyms - click the plus to show
This variation has 19 HGVS names - click the plus to show
This variation has assays on: Illumina_ExomeChip
This variant overlaps 15 transcripts.