Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.01 (C)
Location

Chromosome 11:111908161 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.111908161A>C

About this variant

This variant overlaps 19 transcripts and has 2505 individual genotypes.

Variation displays