Original source

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

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

Chromosome X:150563875-150563879 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.150563875_150563879delTCTTT

Variation displays