Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variants

HGMD-PUBLIC CM043882, CM062036

Most severe consequence
Missense variant
Evidence status

Clinical significance


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

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays