Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.13 (A)
Location

Chromosome 7:30969071 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM005494

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

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

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 3361 individual genotypes, is associated with 1 phenotype and is mentioned in 9 citations.

Variation displays