Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.39 (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 1376 individual genotypes and is mentioned in 2 citations.

Variation displays