Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.15 (C)
Location

Chromosome 13:27639413 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60791154, rs1747179

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 3034 sample genotypes.

Variant displays