Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.49 (G)

Chromosome 12:10383559 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs2617155, rs17809135

HGVS names

This variant has 20 HGVS names - Show

About this variant

This variant overlaps 20 transcripts and has 2578 sample genotypes.

Variant displays