Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome X:19357664 (forward strand) | View in location tab

Co-located

with COSMIC COSM1740794 (A/C), COSM1740793 (A/C) ; HGMD-PUBLIC CM950922

Most severe consequence
 
Start lost
Evidence status

Clinical significance

This variant has 7 synonyms - click the plus to show

This variant has 13 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 15 transcripts, has 607 sample genotypes, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays