Original source

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

G/T | Ancestral: C | Ambiguity code: K | MAF: 0.48 (T)

Chromosome X:151397088 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs524885

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

About this variant

This variant overlaps 4 transcripts and has 1097 individual genotypes.

Variation displays