Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.12 (A)
Location

Chromosome 11:116837538 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR961720

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61758320, rs17249491

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 2529 individual genotypes and is mentioned in 5 citations.

Variation displays