Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.42 (T)
Location

Chromosome 12:132636864 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17771627, rs60275652

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2939 sample genotypes.

Variant displays