Original source

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

Alleles
TTA/- | MAF: 0.01 (-)
Location

Chromosome X:134458894-134458896 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.134458894_134458896delTTA

Variation displays