Original source

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

Alleles
C/A|Ancestral: A|Ambiguity code: M|MAF: 0.25 (A)
Location

Chromosome 12:53721840 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs17102164, rs2293443

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 20 transcripts and has 2762 sample genotypes.

Variant displays