Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.34 (A)
Location

Chromosome 11:66067780 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs57700903

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2510 sample genotypes.

Variant displays