Original source

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

Alleles
C/G|Ancestral: G|Ambiguity code: S|MAF: 0.39 (C)
Location

Chromosome 11:72245855 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

11:g.72245855C>G

About this variant

This variant overlaps 4 transcripts and has 2780 sample genotypes.

Variant displays