Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.40 (A)
Location

Chromosome 11:69775191 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

11:g.69775191A>G
ENST00000168712.2:c.-107T>C

About this variant

This variant overlaps 3 transcripts and has 2510 individual genotypes.

Variation displays