Original source

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

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.09 (C)

Chromosome X:115012128 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs6655306

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

About this variant

This variant overlaps 3 transcripts and has 1408 individual genotypes.

Variation displays