Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.29 (A)
Location

Chromosome 4:186199471 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60216991

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2511 sample genotypes.

Variant displays