Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.30 (G)
Location

Chromosome 11:66187673 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs1190942, rs1151535, rs1191203

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2512 sample genotypes.

Variant displays