Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

T/G|Ancestral: G|Ambiguity code: K|MAF: 0.35 (G)

Chromosome X:78122769 (forward strand)|View in location tab

Co-located variant

dbSNP rs551520954 (T/G)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs386556435

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 4 transcripts and has 3596 sample genotypes.

Variant displays