Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.40 (C)
Location

Chromosome 11:68343621 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

About this variant

This variant overlaps 3 transcripts, has 2548 individual genotypes and is mentioned in 2 citations.

Variation displays