Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.13 (T)
Location

Chromosome 9:6016125 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

9:g.6016125C>T

About this variant

This variant overlaps 4 transcripts and has 2505 individual genotypes.

Variation displays