Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.36 (A)
Location

Chromosome 15:74041072 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61518227

This variant has 7 HGVS names - click the plus to show

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 16 transcripts, 1 regulatory feature, has 4325 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays