Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.05 (A)
Location

Chromosome 4:89726127 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR094129

Most severe consequence
Evidence status

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts, has 2937 individual genotypes and is mentioned in 5 citations.

Variation displays