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:2787284 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM941303

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8615, 2010_April_001_008_SRY_480000_0010

This variation has 5 HGVS names - click the plus to show

Variation displays