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 17:63917810 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM012951, CM067672

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

Uniprot VAR_011919

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 7 transcripts, has 2776 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays