Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: < 0.01 (C)
Location

Chromosome 19:52188128 (forward strand) | View in location tab

Most severe consequence
HGVS name

19:g.52188128G>C

About this variant

This variant overlaps 6 transcripts and has 2504 individual genotypes.

Variation displays