Original source

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

Alleles
-/TCCCCT | MAF: 0.29 (TCCCCT)
Location

Chromosome 5: between 181236805 and 181236806 (forward strand) | View in location tab

Most severe consequence
HGVS name

5:g.181236805_181236806insTCCCCT

Variation displays