Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

G/A|Ambiguity code: R

Chromosome Y:2787207 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM971423, CM068437

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 8624, 2010_April_001_015_SRY_480000_0019

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays