Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.18 (G)
Location

Chromosome 6:135105435 (forward strand) | View in location tab

Co-located
Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

HGVS name

6:g.135105435A>G

This variation has assays on 15 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2512 individual genotypes, is associated with 6 phenotypes and is mentioned in 30 citations.

Variation displays