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 14:88384469 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

14:g.88384469G>C

About this variant

This variant overlaps 18 transcripts and has 2505 individual genotypes.

Variation displays