Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/A | Ambiguity code: W
Location

Chromosome Y:2787287 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920650

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8612, 2010_April_001_006_SRY_480000_0007

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

Variation displays