Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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


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 1525 individual genotypes and is mentioned in 4 citations.

Variation displays