Original source

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

Alleles
G/- | Ancestral: G | MAF: 0.39 (G)
Location

Chromosome 11:47349934 (forward strand) | View in location tab

Co-located

with dbSNP rs181840234 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

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

About this variant

This variant overlaps 7 transcripts, has 2575 individual genotypes and is mentioned in 1 citation.

Variation displays