Original source

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

Alleles
G/A | Ambiguity code: R
Location

Chromosome Y:2655368 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920649

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8610, 2010_April_001_004_SRY_480000_0005

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

Variation displays