Original source

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

C/- | Ancestral: C | MAF: 0.44 (-)

Chromosome 11:102799765 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2586 sample genotypes, is associated with 4 phenotypes and is mentioned in 67 citations.

Variant displays