Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.45 (C)
Location

Chromosome 13:75587064 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs12866981, rs58838644

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2759 sample genotypes.

Variant displays