Original source

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

C/G | Ancestral: G | Ambiguity code: S | MAF: 0.12 (C)

Chromosome 11:72056550 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs3018309, rs61408328

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and has 2510 sample genotypes.

Variant displays