Original source

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

Alleles
C/T|Ambiguity code: Y
Location

Chromosome Y:2787284 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM941303

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 8615, 2010_April_001_008_SRY_480000_0010

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