Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.01 (C)
Location

Chromosome 22:50568667 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

22:g.50568667T>C

About this variant

This variant overlaps 10 transcripts and has 2505 sample genotypes.

Variant displays