Original source

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

Alleles
C/G | Ancestral: T | Ambiguity code: S | MAF: < 0.01 (G)
Location

Chromosome X:18942302 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

LSDB NM_000292.2:c.1715-50G>C

This variation has 3 HGVS names - click the plus to show

Variation displays