Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs1190942, rs1151535, rs1191203

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2512 sample genotypes.

Variant displays