Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: < 0.01 (G)
Location

Chromosome 6:143939858 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

6:g.143939858T>G

About this variant

This variant overlaps 19 transcripts and has 2504 individual genotypes.

Variation displays