Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.44 (G)
Location

Chromosome 13:113229001 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57902772

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2510 sample genotypes.

Variant displays