Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.35 (T)
Location

Chromosome 1:16987159 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

ClinVar SCV000150364

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2508 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays