Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17036122, rs3202152

This variant has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 35 transcripts and has 2 sample genotypes.

Variant displays