Original source

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

Alleles
TCTTT/- | MAF: < 0.01 (-)
Location

Chromosome X:151395403-151395407 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.151395403_151395407delTCTTT

Variation displays