Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: < 0.01 (G)
Location

Chromosome X:18564539 (forward strand) | View in location tab

Co-located

with PhenCode RettBASE_c.145+17A>G (A/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 145+17A>G

This variation has 7 HGVS names - click the plus to show

Variation displays