Original source

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

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 3097 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays