Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.20 (C)
Location

Chromosome 5:132656717 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR097566

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3756758, rs58550622

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 3732 sample genotypes and is mentioned in 28 citations.

Variant displays