Original source

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

Alleles
C/A/G | Ancestral: C | Ambiguity code: V
Location

Chromosome X:154765450 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042697

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_001363.3:c.91C>G, NM_001363.3:c.91C>A, 6830

This variation has 30 HGVS names - click the plus to show

Variation displays