Original source

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

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

Chromosome 22:50568657 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.50568657C>T

About this variant

This variant overlaps 10 transcripts and has 2504 individual genotypes.

Variation displays