Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.29 (A)
Location

Chromosome 1:230710048 (forward strand) | View in location tab

Co-located

with COSMIC COSM425562 (A/G) ; HGMD-PUBLIC CM920010

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 3817 individual genotypes, is associated with 4 phenotypes and is mentioned in 41 citations.

Variation displays