Original source

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

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

Chromosome 8:43199410 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs386517918, rs61686361

This variant has 4 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 2512 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays