Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 1:149261767 (forward strand) | View in location tab
This variation has 2 HGVS names - click the plus to show
This variation has assays on: Illumina_ExomeChip
This variant overlaps 4 transcripts.