Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.07 (G)
Location

Chromosome 19:42325119 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.42325119T>G

About this variant

This variant overlaps 8 transcripts and has 2504 individual genotypes.

Variation displays