Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.07 (T)
Location

Chromosome 12:1913567 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17223603, rs58820222

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2851 sample genotypes.

Variant displays