Original source

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

Alleles
C/A/T|Ambiguity code: H|MAF: 0.37 (C)
Location

Chromosome 11:18397987 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61359575

HGVS names

This variant has 42 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 50 transcripts and has 3693 sample genotypes.

Variant displays