Original source

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

Alleles
A/C|Ancestral: C|Ambiguity code: M|MAF: 0.46 (A)
Location

Chromosome 11:69809515 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs74235985

HGVS name

11:g.69809515A>C

About this variant

This variant overlaps 1 transcript and has 2661 sample genotypes.

Variant displays