Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 4:6302385 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM043882, CM062036

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_006005.2:c.2590G>A, 2010_April_001_095_WFS1_606201_0020, 13641

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variation displays