Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.13 (A)
Location

Chromosome 19:33301725 (forward strand) | View in location tab

Co-located

with COSMIC COSM3756627 (C/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_004364.3:c.690G>T

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 2504 individual genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays