Original source

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

Alleles
G/A | Ambiguity code: R
Location

Chromosome Y:2787600 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981858

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_016_SRY_480000_0020, 8625

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

Y:g.2787600G>A
ENST00000383070.1:c.4C>T
ENSP00000372547.1:p.Gln2Ter

Variation displays