Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
CCCTCAGACCCAGGAGTCCAGACTCCAGCTCCTCCT/-
Location

Chromosome 19:55546982-55547017 (forward strand) | View in location tab

Most severe consequence
Synonyms

Archive dbSNP rs36230155

HGVS name

19:g.55546982_55547017delCCCTCAGACCCAGGAGTCCAGACTCCAGCTCCTCCT

Variation displays