This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/A/G/T | Ancestral: C | Ambiguity code: N | MAF: 0.34 (A)

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

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs57700903

HGVS names

This variant has 21 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and has 2632 sample genotypes.

Variant displays