Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D|MAF: 0.11 (T)
Location

Chromosome 7:30974242 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57292284

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 20 transcripts, has 2508 sample genotypes and is mentioned in 1 citation.

Variant displays