Original source

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

T/C | Ancestral: T | Ambiguity code: Y

Chromosome X:101010404 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and is mentioned in 1 citation.

Variant displays