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
Evidence status

Synonyms

LSDB FEVR_43

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

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 5 transcripts and is mentioned in 1 citation.

Variation displays