Original source

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

Alleles
T/A|Ambiguity code: W
Location

Chromosome Y:2787330 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM920648

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_012_SRY_480000_0015, 8620

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays