Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 1:17005754 (forward strand) | View in location tab
with HGMD-PUBLIC CM071562
This variation has 10 HGVS names - click the plus to show
This variation has assays on: Illumina_ExomeChip
This variant overlaps 10 transcripts.