Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.22 (A)
Location

Chromosome 3:171014511 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM941277

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

This variation has assays on 13 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2632 individual genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variation displays