Original source

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

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

Chromosome 11:67490807 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS083216

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_003977.2:c.807C>T

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts, has 2504 individual genotypes and is associated with 1 phenotype.

Variation displays