Original source

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

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

Chromosome 18:5392241 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

18:g.5392241T>C

About this variant

This variant overlaps 11 transcripts and has 2505 individual genotypes.

Variation displays