Original source

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

A/G | Ancestral: A | Ambiguity code: R

Chromosome 1:11021885 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17036122, rs3202152

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 35 transcripts and has 2 sample genotypes.

Variant displays