Original source

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

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

Chromosome 1:11022301 (forward strand) | View in location tab


with HGMD-PUBLIC CM083177

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 25 HGVS names - click the plus to show

About this variant

This variant overlaps 35 transcripts, has 1 individual genotype, is associated with 3 phenotypes and is mentioned in 1 citation.

Variation displays