Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: < 0.01 (T)
Location

Chromosome 11:68357679 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM041034

Most severe consequence
 
Missense variant
Evidence status

Synonyms

LSDB FEVR_29

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 2 transcripts, has 2504 sample genotypes and is mentioned in 1 citation.

Variant displays