Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.16 (A)

Chromosome 1:11019901 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60982353

HGVS names

This variant has 21 HGVS names - Show

About this variant

This variant overlaps 34 transcripts and has 2509 sample genotypes.

Variant displays