Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.12 (A)
Location

Chromosome 11:65796564 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs386596394, rs3897551

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

This variation has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2603 individual genotypes.

Variation displays