Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.07 (C)
Location

Chromosome 18:31598550 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 2505 individual genotypes, is associated with 1 phenotype and is mentioned in 3 citations.

Variation displays