Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.18 (T)
Location

Chromosome 5:135032479 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386603770, rs61154969

This variant has 6 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2599 sample genotypes and is mentioned in 1 citation.

Variant displays