Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: < 0.01 (G)
Location

Chromosome 11:68411509 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM053296

Most severe consequence
 
Missense variant
Evidence status

Synonyms

LSDB FEVR_39

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2504 sample genotypes and is mentioned in 1 citation.

Variant displays