Original source

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

Alleles
G/A | Ambiguity code: R
Location

Chromosome Y:2655248 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971423, CM068437

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8624, 2010_April_001_015_SRY_480000_0019

This variation has 7 HGVS names - click the plus to show

Variation displays