Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.31 (A)
Location

Chromosome 12:75479883 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs57486361

HGVS name

12:g.75479883C>A

About this variant

This variant overlaps 5 transcripts and has 2579 sample genotypes.

Variant displays