Original source

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

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

Chromosome X:50003843 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56766896

This variation has 4 HGVS names - click the plus to show

Variation displays