Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.14 (C)
Location

Chromosome 11:76933103 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60250906

This variation has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 2508 individual genotypes.

Variation displays