Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.21 (C)
Location

Chromosome Y:12699311 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

Y:g.12699311G>C

About this variant

This variant overlaps 2 transcripts and has 1234 sample genotypes.

Variant displays