Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 11:120267657 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs4285878, rs60107070

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 6 sample genotypes.

Variant displays