Original source

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

Alleles
T/A | Ambiguity code: W
Location

Chromosome Y:2787224 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM941304, CM021699

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_019_SRY_480000_0023, 8628

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and is associated with 2 phenotypes.

Variation displays