This variation has been flagged
Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]
Chromosome 19:48974919 (forward strand) | View in location tab
with dbSNP rs144426771 (T/C)
Archive dbSNP rs74389437
This variation has 14 HGVS names - click the plus to show
This variant overlaps 15 transcripts.