Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

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

Most severe consequence
Evidence status

HGVS name

Y:g.12699311G>C

About this variant

This variant overlaps 2 transcripts and has 1 individual genotype.

Variation displays