Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 1:16991749 (forward strand) | View in location tab
with HGMD-PUBLIC CM085956
This variation has 11 HGVS names - click the plus to show
This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12
This variant overlaps 12 transcripts.