Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.41 (T)
Location

Chromosome 3:50190438 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

3:g.50190438C>T

About this variant

This variant overlaps 9 transcripts and has 2507 individual genotypes.

Variation displays