Original source

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

Alleles
C/T | Ambiguity code: Y
Location

Chromosome Y:2787320 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM004706

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_018_SRY_480000_0022, 8627

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

Variation displays