Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 11:68436969 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041036

Most severe consequence
 
Missense variant
Evidence status

Synonyms

LSDB FEVR_43

This variant has 4 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and is mentioned in 1 citation.

Variant displays