Original source

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

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

Chromosome 1:11018836 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM081838

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 37 HGVS names - click the plus to show

About this variant

This variant overlaps 32 transcripts, is associated with 3 phenotypes and is mentioned in 1 citation.

Variation displays